FDA device listing
45017, 45018, 45019, 45023, 45025, 45027, 45028, 45029, 45030, 45031,4900-LR-2, 4900-SK…
FDA device listing 1605451580 · VIETNAM YETITECH EQUIPMENT COMPANY LIMITED
Key facts
| Proprietary names | 45017, 45018, 45019, 45023, 45025, 45027, 45028, 45029, 45030, 45031,4900-LR-2, 4900-SK, 100630-100,100630-200,100678-000, 100689-100,Neoprene Knee Support:45003, 45005, 45007, 45008, 45009, 45013,OA Knee Brace: 49001, 49002, 4900-WR, 4900-KEY, 4900-BS-2, 4900-FS, 4900-LL-2 |
|---|---|
| Owner/operator | VIETNAM YETITECH EQUIPMENT COMPANY LIMITED |
| Owner/operator number | 10089165 |
| Product codes | ITQ |
| Device names | ITQ - Joint, Knee, External Brace |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| Review panels | Physical Medicine |
| Registered establishments | VIETNAM YETITECH EQUIPMENT COMPANY LIMITED |
| Establishment registrations | 3030175335 |
| FEI numbers | 3030175335 |
| Establishment operations | Foreign Exporter, 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