FDA device listing
DYNA LIMITED MOTION KNEE BRACE PREMIUM,DYNA LIMITED MOTION KNEE BRACE( ROM BRACE),DYNA ROM ELBOW BRACE
FDA device listing 1520241575 · DYNAMIC TECHNO MEDICALS PRIVATE LIMITED
Key facts
| Proprietary names | DYNA LIMITED MOTION KNEE BRACE PREMIUM,DYNA LIMITED MOTION KNEE BRACE( ROM BRACE),DYNA ROM ELBOW BRACE |
|---|---|
| Owner/operator | DYNAMIC TECHNO MEDICALS PRIVATE LIMITED |
| Owner/operator number | 10039773 |
| Product codes | IRD |
| Device names | IRD - Joint, Elbow, External Limb Component, Mechanical |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3420 |
| Review panels | Physical Medicine |
| Registered establishments | DYNAMIC TECHNO MEDICALS PRIVATE LIMITED |
| Establishment registrations | 3006227741 |
| FEI numbers | 3006227741 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database