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Chisel, Surgical, Manual

FDA product code FZO · Class 1 · General, Plastic Surgery

1,916
Registered devices
318
Adverse events
1
Recalls
2
510(k) clearances

Devices with this code

Sklar® — SKLAR CORPORATIONAmbler Surgical — AMBLER SURGICAL CORP.L-Box® — INNO Holdings, Inc.Surtex — SURTEX INSTRUMENTS LTD.Vital Spinal Fixation System — Highridge Medical, LLCRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHRENOVATION — Smith & Nephew, Inc.X-Box — INNO Holdings, Inc.Surtex — SURTEX INSTRUMENTS LTD.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONSklar® — SKLAR CORPORATIONTimberline Lateral Fusion System — Highridge Medical, LLCV. Mueller — CAREFUSION 2200, INCBOSS Instruments — BOSS INSTRUMENTS, LTD., INC.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftSklar® — SKLAR CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONBOSS Instruments — BOSS INSTRUMENTS, LTD., INC.Intervertebral Disc Preparation Instruments — ALPHATEC SPINE, INC.CHISEL — KLS-Martin L.P.NA — Fehling Instruments GmbH & Co. KGSklar® — SKLAR CORPORATIONSymmetry U.S. Army — ASPEN SURGICAL PRODUCTS, INC.Timberline Lateral Fusion System — Highridge Medical, LLC

Recent recalls

DateFirmReason
2015-06-24Synthes (USA) Products LLCIt was discovered that a 10mm Chisel Blade was etched as a 16mm Chisel Blade.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.