Skip to content

Ace 5100017

by Ace Surgical Supply Co., Inc.

Ace 5100017 is a Class I device made by Ace Surgical Supply Co., Inc., listed in FDA GUDID since 5 Dec 2023 (UDI-DI 00614950031245), 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 Number00614950031245 UDI-DI Date5 Dec 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  • Withdrawn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
Ace
Generic name
Dental dressing forceps, reusable
Model / Ref / Catalog
5100017
Primary DI / UDI-DI
00614950031245
FDA product code
EMH
GMDN term
Dental dressing forceps, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental dressing forceps, reusable

Other devices from Ace Surgical Supply Co., Inc.

See all devices from Ace Surgical Supply Co., Inc. →

Properties

  • Supplied sterile
  • Prescription use
  • Premarket exempt
Other properties (12, all answered No)