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Extraction Forceps Fig. 1

by Melpex Beauty Instruments GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08961104670006 UDI-DIDate12 May 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Extraction Forceps
Generic Name
Tooth extraction forceps
Model / Ref / Catalog
Fig. 1, 305-002
Primary DI / UDI-DI
08961104670006
FDA Product Code
EMG
GMDN Term
Tooth extraction forceps
Device Class
Class I
Regulation Number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Melpex Beauty Instruments

See all devices from Melpex Beauty Instruments →

Properties

  • Sterile
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No