FDA device listing
DYNA BUNION BRACE,DYNA FINGER EXTENSION BRACE,DYNA FROG SPLINT,DYNA LIMB RESTRAINER,OLYMPIAN THIGH SUPPORT,Tender…
FDA device listing 1578314327 · DYNAMIC TECHNO MEDICALS PRIVATE LIMITED
Key facts
| Proprietary names | DYNA BUNION BRACE,DYNA FINGER EXTENSION BRACE,DYNA FROG SPLINT,DYNA LIMB RESTRAINER,OLYMPIAN THIGH SUPPORT,Tender Shoulder care |
|---|---|
| Owner/operator | DYNAMIC TECHNO MEDICALS PRIVATE LIMITED |
| Owner/operator number | 10039773 |
| Product codes | IQI |
| Device names | IQI - Orthosis, Limb Brace |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| 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