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Trinity Sterile, Inc. 20665SF

by Trinity Sterile, Inc.

Trinity Sterile, Inc. 20665SF is a Class I device made by Trinity Sterile, Inc., listed in FDA GUDID since 28 Jul 2023 (UDI-DI 10841767102845), 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 Number10841767102845 UDI-DI Date28 Jul 2023ListedStatusListed 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  • Withdrawn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
Trinity Sterile, Inc.
Generic name
Circumcision kit, single-use
Model / reference
20665SF
Primary DI / UDI-DI
10841767102845
FDA product code
LRP
GMDN term
Circumcision kit, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Circumcision kit, single-use

Other devices from Trinity Sterile, Inc.

See all devices from Trinity Sterile, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (9, all answered No)