FDA device listing
Bite Block, Conmed
FDA device listing 1974882529 · CONMED CORPORATION
Key facts
| Proprietary names | Bite Block, Conmed |
|---|---|
| Owner/operator | CONMED CORPORATION |
| Owner/operator number | 1317214 |
| Product codes | MNK |
| Device names | MNK - Endoscopic Bite Block |
| Device class | Class I |
| Classification regulations (21 CFR) | 876.1500 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | Conmed Corporation, CONMED CORPORATION, Consolidated Medical Equipment Company |
| Establishment registrations | 1223925, 1320894, 3007305485 |
| FEI numbers | 1000305720, 3001451571, 3007305485 |
| Establishment operations | Complaint File Establishment, Contract Manufacturer, Specification Developer |
| 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