FDA device listing
Anderson Bear Claw Retractors 3 sharp, prongs 11 cm,Anderson Bear Claw Retractors 3 sharp, prongs 12 cm,Anderson Bear…
FDA device listing 1108513663 · Stellmacher Instruments Inc
Key facts
| Proprietary names | Anderson Bear Claw Retractors 3 sharp, prongs 11 cm,Anderson Bear Claw Retractors 3 sharp, prongs 12 cm,Anderson Bear Claw Retractors 3 sharp, prongs 16 cm,Anderson Bear Claw Retractors 3 sharp, prongs 7 cm,Anderson Bear Claw Retractors 7 sharp, prongs 11 cm,Anderson Bear Claw Retractors 7 sharp, prongs 12 cm,Anderson Bear Claw Retractors 7 sharp, prongs 16 cm,Anderson Bear Claw Retractors 7… |
|---|---|
| Owner/operator | Stellmacher Instruments Inc |
| Owner/operator number | 10088967 |
| Product codes | GAD |
| Device names | GAD - Retractor |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | STELLMACHER INSTRUMENTS INC |
| Establishment registrations | 3029754081 |
| FEI numbers | 3029754081 |
| Establishment operations | Repackager/Relabeler |
| 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