FDA device listing
Q-FIX ALL-SUTURE ANCHOR
FDA device listing 1790542662 · Diafarma Ecza Deposu ve Medikal Dis Ticaret Dis Tic Ltd Sti
Key facts
| Proprietary names | Q-FIX ALL-SUTURE ANCHOR |
|---|---|
| Owner/operator | Diafarma Ecza Deposu ve Medikal Dis Ticaret Dis Tic Ltd Sti |
| Owner/operator number | 10060275 |
| Premarket submissions | K133727 |
| Product codes | MBI |
| Device names | MBI - Fastener, Fixation, Nondegradable, Soft Tissue |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3040 |
| Review panels | Orthopedic |
| Registered establishments | DIAFARMA ECZA DEPOSU VE MEDIKAL DIS TICARET DIS TIC LTD STI |
| Establishment registrations | 3011989923 |
| FEI numbers | 3011989923 |
| Establishment operations | Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 10–99 Device listings citing the same submission
- Yes 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