Atlas FDA

EMG

10 FDA 510(k) clearances · Product code

57 daysmedian time to decision
264 days90th percentile
10clearances measured

FDA profile

Official device name
Forceps, Tooth Extractor, Surgical
Device class
Class I (low risk)
Regulation
21 CFR 872.4565
Medical specialty
Dental
Adverse events (MAUDE)
1993: 1 · 2001: 1 · 2002: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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RecordFirmDate
MEISINGER BENEX, MODEL BE001 (K062130)Hager& Meisinger GmbH2007-04-16
EASY X-TRAC SYSTEM (K060691)A. Titan Instruments, Inc.2006-06-12
500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA (K851708)Artiberia1985-07-01
560 TO 577 VARIOUS TYPES OF FORCEPS FOR CHILDREN (K851709)Artiberia1985-06-11
600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI (K851712)Artiberia1985-06-11
600/7 TO 600/288 VARIOUS TYPES OF AMER. PATTERN DE (K851711)Artiberia1985-06-11
TOOTH EXTRACTING FORCEPS 151(2010)-875 PCS. SS410/ (K851105)The Huxley Instrument Corp.1985-05-15
CAT. 8 DENTAL DEVICES (K840312)Imm Enterprises , Ltd.1984-04-05
DENTAL INSTRUMENTS - SURGICAL FORCEPS (K823325)Miltex, Inc.1982-11-24
BEACH FORCEP NO. 150 AND NO. 151 (K821781)Pacific Dental Corp.1982-07-02

Track EMG automatically

Every clearance here is in the API, with alerts when new ones post.