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Sterling 5821-121

by Benco Dental Supply Co.

Sterling 5821-121 is a Class I device made by Benco Dental Supply Co., listed in FDA GUDID since 4 Aug 2022 (UDI-DI 00366975064004), 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 Number00366975064004 UDI-DI Date4 Aug 2022ListedStatusListed 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  • Withdrawn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
Dental cheek retractor, professional, reusable
Model / reference
5821-121
Primary DI / UDI-DI
00366975064004
FDA product code
EIG
GMDN term
Dental cheek retractor, professional, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental cheek retractor, professional, reusable

Other devices from Benco Dental Supply Co.

See all devices from Benco Dental Supply Co. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)