FD-3000™ Flexion Distraction Device
FD-3000™ flexion distraction device is TheraMod’s table-assisted rehabilitation device for trained clinical, chiropractic, physiotherapy, and musculoskeletal care settings.
The device was developed around controlled table movement, patient positioning, guided setup, user training, documentation, service planning, and distributor support.
FD-3000™ is part of TheraMod’s current rehabilitation equipment portfolio, alongside RxDecom® and Spinercise®. Within that portfolio, FD-3000™ represents the flexion-distraction and table-assisted rehabilitation category.
We are registered with the Medical Device Authority (MDA), hold a medical device manufacturing licence, and operate under an ISO 13485-certified quality management system certified by TÜV SÜD. TheraMod publishes licence numbers, registration details, and certificate references where available.
Key Takeaways About FD-3000™
Area | Summary |
|---|---|
Device | FD-3000™ |
Category | Flexion-distraction rehabilitation device |
Intended setting | Trained clinical and rehabilitation environments |
Main design | Motorized power table, cushioned surface, adjustable headpiece, thoracolumbar section, moveable pelvic section |
Buyer relevance | Clinics, distributors, investors, rehabilitation groups |
Portfolio role | TheraMod’s table-assisted rehabilitation category |
Use position | Professional equipment, not general consumer equipment |
FD-3000™ Device Overview
A flexion-distraction device is a table-assisted equipment category used in trained professional environments.
The category is commonly associated with sectioned table design, controlled table movement, body positioning, guided setup, and professional user training.
The FD-3000™ is described here through its design and its intended setting. This page does not make treatment promises or broad clinical claims.
FD-3000™ registration
- Device
- FD-3000™
- Registration number
- GA6416424-169842
- Class
- Class A
- Manufacturer
- TheraMod (M) Sdn. Bhd.
- Establishment licence
- MDA-5532-K124
- Quality system
- ISO 13485
Registration and certification are regulatory and quality-system facts. They do not establish clinical outcomes, comparative superiority, authorization in another market, or MDA endorsement.
What Is a Flexion-Distraction Device?
A flexion-distraction device is a table-assisted equipment category used in trained professional environments.
The category is commonly associated with sectioned table design, controlled table movement, body positioning, guided setup, and professional user training.
The FD-3000™ is described here through its design and its intended setting. This page does not make treatment promises or broad clinical claims.
Table-Assisted Design
The table-assisted design is the main product identity of FD-3000™.
Professional rehabilitation equipment must be practical in daily use. FD-3000™ was developed to support controlled table movement, setup guidance, positioning, and structured workflow in trained environments.
This makes FD-3000™ different from RxDecom®, which represents spinal decompression equipment, and Spinercise®, which represents movement-based rehabilitation.
Technical Structure
FD-3000™ includes:
- Motorized power table
- Cushioned table surface
- Adjustable headpiece
- Stationary thoracolumbar section
- Moveable pelvic section
- Table-assisted movement design
These features define FD-3000™ as a flexion-distraction rehabilitation device rather than a general treatment table.
For distributors and investors, the technical structure should be reviewed together with manufacturing repeatability, servicing, maintenance, user training, and documentation.
Professional-Use Setting
FD-3000™ is intended for trained clinical and rehabilitation environments.
Suitable settings may include rehabilitation centers, physiotherapy centers, chiropractic centers, hospital-linked rehabilitation departments, and musculoskeletal care settings.
Use, availability, claims, and regulatory status should be reviewed market by market.
How FD-3000™ Fits With Other TheraMod Devices
TheraMod’s current device portfolio includes RxDecom®, Spinercise®, and FD-3000™.
Device | Category | Portfolio Role |
|---|---|---|
RxDecom® | Spinal decompression machine | Spinal decompression equipment |
Spinercise® | Movement rehabilitation device | Guided movement equipment |
FD-3000™ | Flexion-distraction device | Table-assisted rehabilitation equipment |
Together, these devices give TheraMod a broader rehabilitation equipment foundation than a single-product company.
Commercial Relevance
FD-3000™ adds a table-assisted rehabilitation category to TheraMod’s device portfolio.
For investors, FD-3000™ connects to manufacturing growth, product documentation, service planning, training systems, distributor development, and selected market-entry preparation.
Healthcare Professional Notice
FD-3000 information is intended for trained healthcare professionals, procurement teams, qualified distributors, and technical or regulatory reviewers. It is not medical advice or a public product-use guide.
Regulatory Status
FD-3000™ is registered as a Class A FD3000 Powered Table under registration number GA6416424-169842, valid through 27 April 2029.
Registration establishes registered market-access status for the registered device. It does not establish clinical outcomes, comparative superiority, foreign authorization, or MDA/KKM endorsement.
Device Category and Professional Setting
FD-3000 is a professional powered table for trained provider settings. The exact approved intended use, users, operating conditions, indications, contraindications, warnings, and instructions are stated in the current controlled technical file and labelling.
Registered Intended Use and Approved Claims
The registered intended-use statement and approved claims for the FD-3000 are held in the current registration and in the controlled technical file and labelling supplied with the device. Licensed practitioners and institutional buyers can request the current wording from TheraMod using the contact details on this page.
Training and Documentation
FD-3000 is supplied with controlled setup, operating, cleaning, maintenance, safety, service, and user-training materials appropriate to the registered use and market. Training records and competency requirements are maintained where applicable.
Manufacturing and Quality Release
TheraMod retains controlled engineering, bill-of-material, revision, assembly, inspection, regulatory, and final-release records. Any external fabrication output remains subject to TheraMod assembly, inspection, documentation, and quality release.
Service, Maintenance, and Warranty
Professional buyers should receive clear written information regarding installation, maintenance, spare parts, service response, complaint escalation, warranty terms, and record retention. Commercial details depend on the market and executed agreement.
Procurement and Distributor Information
Qualified buyers and distributors may request current registration evidence, controlled product documentation, training and installation requirements, service planning, and written quotation. Market entry and availability remain jurisdiction-specific.
Availability
Availability depends on current registration, authorized distribution, written terms, installation, user training, and service capability. This page does not invite general-public purchase or use.
Distributor Relevance
FD-3000™ may be relevant to distributor discussions involving rehabilitation equipment, chiropractic equipment, physiotherapy equipment, table-assisted devices, training, servicing, installation guidance, and country-specific regulatory review.
Distributors should review product category fit, intended setting, service requirements, training needs, documentation, pricing pathway, local regulatory requirements, and country-specific market planning.
Investor Information
TheraMod is preparing for its next growth stage through medical device manufacturing, product-line expansion, regulatory preparation, distributor development, training systems, service planning, and new market entry.
Our current device portfolio includes RxDecom®, Spinercise®, and FD-3000™, with additional musculoskeletal devices in R&D.
Investors, strategic partners, manufacturers, healthcare groups, and distributor groups may review the dedicated investor page for more information.
Frequently Asked Questions
What is FD-3000™?
What type of device is FD-3000™?
Is FD-3000™ the same as RxDecom®?
Is FD-3000™ the same as Spinercise®?
Is FD-3000™ intended for general public use?
Why is FD-3000™ relevant to investors?
What should distributors review before discussing FD-3000™?
Where can investors learn more?
Page Summary
FD-3000™ is TheraMod’s flexion-distraction rehabilitation device for trained clinical, chiropractic, physiotherapy, and musculoskeletal care settings.
Professional buyers and distributors can request FD-3000™ specifications, installation requirements and training details through the TheraMod contact page.
The device should be reviewed through its table-assisted design, motorized power table, cushioned surface, adjustable headpiece, thoracolumbar section, moveable pelvic section, documentation, service planning, training requirements, distributor pathway, and manufacturing readiness.
As part of TheraMod’s current rehabilitation equipment portfolio, FD-3000™ supports our wider direction in medical device manufacturing, distributor development, technical training, service readiness, and the FD-3000 flexion distraction device category.
Author
Yama Zafer, D.C., author of “FD-3000 Powered Table | Healthcare Professional Information,” is the Founder and Managing Director of TheraMod (M) Sdn. Bhd.; read his TheraMod corporate biography.
Related Pages
Last Updated and Reviewed
“FD-3000 Registered Class A Powered Table” was reviewed and updated on 1 September 2026 to reflect the current corporate, regulatory, quality-system, product-stage, and document-control information supplied for TheraMod.
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