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Sterling 1676-591

by Benco Dental Supply Co.

Sterling 1676-591 is a Class I device made by Benco Dental Supply Co., listed in FDA GUDID since 21 Sep 2018 (UDI-DI 00366975023131), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00366975023131 UDI-DI Date21 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
Periosteal elevator, reusable
Model / reference
1676-591
Primary DI / UDI-DI
00366975023131
FDA product code
EMJ
GMDN term
Periosteal elevator, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Periosteal elevator, reusable

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 (12, all answered No)