FDA device listing
10MM CANNULATED DRILL,11MM CANNULATED DRILL,12MM CANNULATED DRILL,13MM CANNULATED DRILL,2.0MM DRILL BIT,3.2MM CANNULATED…
FDA device listing 1229682732 · Celestica de Monterrey S.A. de C.V.
Key facts
| Proprietary names | 10MM CANNULATED DRILL,11MM CANNULATED DRILL,12MM CANNULATED DRILL,13MM CANNULATED DRILL,2.0MM DRILL BIT,3.2MM CANNULATED DRILL,3.2MM TWIST DRILL BIT 5 INCH,3/32 GUIDE PIN FOR FEMORAL AIMER, 25 PACK,3.5MM HEX BIT NON-CANN,3.7MM CANNULATED DRILL,4.5MM CANN TOGGLE BUTTON DRILL,5.5MM CANNULATED DRILL,5MM ALLTHREAD TI DRILL,5MM CANNULATED DRILL,6.5MM CANNULATED DRILL,6MM CANNULATED DRILL,7.5MM… |
|---|---|
| Owner/operator | Celestica de Monterrey S.A. de C.V. |
| Owner/operator number | 10054863 |
| Product codes | HTW |
| Device names | HTW - Bit, Drill |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.4540 |
| Review panels | Orthopedic |
| Registered establishments | CELESTICA de MONTERREY S.A. de C.V. |
| Establishment registrations | 3003139373 |
| FEI numbers | 3003139373 |
| Establishment operations | Contract 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