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Sterling 4031-950

by Benco Dental Supply Co.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00366975023537 UDI-DI Date21 Sep 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Sterling
Generic Name
Tooth extraction forceps
Model / Reference
4031-950
Primary DI / UDI-DI
00366975023537
FDA Product Code
EMG
GMDN Term
Tooth extraction forceps
Device Class
Class I
Regulation Number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Tooth extraction forceps

Other devices from Benco Dental Supply Co.

See all devices from Benco Dental Supply Co. →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

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