FDA Device Intelligence
Home › Device types › EMG

Forceps, Tooth Extractor, Surgical

FDA product code EMG · Class 1 · Dental

3,590
Registered devices
11
Adverse events
1
Recalls
10
510(k) clearances

Devices with this code

devemed — devemed GmbHV. Mueller — STERIS CORPORATIONSTERLING — BENCO DENTAL SUPPLY CO.HELMUT ZEPF — Helmut Zepf Medizintechnik GmbHEXTRACTION FORCEPS #962 UPPER DLC — W.H. Holden, Inc.Nordent Manufacturing, Inc. — NORDENT MANUFACTURING INCMedicon — Medicon eG. Chirurgiemechaniker-Genossenschaftdevemed — devemed GmbHBMT Medizintechnik GmbH — BMT Medizintechnik GmbHEXTRACTION FORCEPS #151 DIAMOND — W.H. Holden, Inc.EXTRACTION FORCEPS #22 LOWER MOLAR — W.H. Holden, Inc.devemed — devemed GmbHdevemed — devemed GmbHdevemed — devemed GmbHIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONPower Dental USA — Power Dental U.S.A. Inc.BMT Medizintechnik GmbH — BMT Medizintechnik GmbHPower Dental USA — Power Dental U.S.A. Inc.Karl Schumacher — Karl Schumacher Dental, LLCHELMUT ZEPF — Helmut Zepf Medizintechnik GmbHdevemed — devemed GmbHA. Titan Instruments — A. TITAN INSTRUMENTS, INC.N/A — BIOMET MICROFIXATION, INCDental — TIMESCO HEALTHCARE LIMITED

Recent recalls

DateFirmReason
2008-05-21Biomet Microfixation, Inc.The Biomet Microfixation Obwegeser Ramus Clamp, Wide Right 01-7996 were incorrectly etched as the left part number 01-7997.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.