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Table, Operating-Room, Manual
FDA product code FSE · Class 1 · General, Plastic Surgery
103
Registered devices
28
Adverse events
1
Recalls
13
510(k) clearances
Devices with this code
C-Thru — INSTRUMENT SPECIALISTS, INC.SchureMed — SCHUERCH CORPORATIONISI — INSTRUMENT SPECIALISTS, INC.SchureMed — SCHUERCH CORPORATIONC-Thru — INSTRUMENT SPECIALISTS, INC.Hunter Medical — INSTRUMENT SPECIALISTS, INC.ISI — INSTRUMENT SPECIALISTS, INC.C-Thru — INSTRUMENT SPECIALISTS, INC.ISI — INSTRUMENT SPECIALISTS, INC.ISI — INSTRUMENT SPECIALISTS, INC.ISI — INSTRUMENT SPECIALISTS, INC.SchureMed — SCHUERCH CORPORATIONISI — INSTRUMENT SPECIALISTS, INC.ISI — INSTRUMENT SPECIALISTS, INC.Carter — INSTRUMENT SPECIALISTS, INC.BETACLASSIC — Maquet (Suzhou) Co. LTDISI — INSTRUMENT SPECIALISTS, INC.ISI — INSTRUMENT SPECIALISTS, INC.SchureMed — SCHUERCH CORPORATIONISI — INSTRUMENT SPECIALISTS, INC.ISI — INSTRUMENT SPECIALISTS, INC.C-Thru — INSTRUMENT SPECIALISTS, INC.ISI — INSTRUMENT SPECIALISTS, INC.Carter — INSTRUMENT SPECIALISTS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-05-15 | Stryker Medical Div. of Stryker Corporation | An incorrect pin may have been used during assembly and therefore the device may give way during use. |
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