510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
EMGClass I

Forceps, Tooth Extractor, Surgical

21 CFR 872.4565 / Dental
FDA source (opens on fda.gov)

EMG is the FDA product code for Forceps, Tooth Extractor, Surgical, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold 10 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
EMG
Device name
Forceps, Tooth Extractor, Surgical
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
10
Ingested recalls
1

Clearances, product code EMG

By decision year
10 clearances under product code EMG with a decision year between 1982 and 2007, 1985 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code EMG by decision year
YearClearances
19822
19841
19855
20061
20071

Applicants with the most clearances

Product code EMG
Applicants holding the most 510(k) clearances under product code EMG
ApplicantClearances
Artiberia4
A. Titan Instruments, Inc.1
Hager & Meisinger GmbH1
Imm Enterprises, Ltd.1
Miltex, Inc.1
Pacific Dental Corp.1
The Huxley Instrument Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 210 companies shown, in name order