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Ace 1000025

by Ace Surgical Supply Co., Inc.

Ace 1000025 is a Class I device made by Ace Surgical Supply Co., Inc., listed in FDA GUDID since 24 Oct 2019 (UDI-DI 00614950023592), 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 Number00614950023592 UDI-DI Date24 Oct 2019ListedStatusListed 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  • Withdrawn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 rongeur
Model / Ref / Catalog
1000025
Primary DI / UDI-DI
00614950023592
FDA product code
EMH
GMDN term
Dental rongeur
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 6 Inch

Similar devices

Other devices filed under FDA product code EMH (FORCEPS, RONGEUR, SURGICAL).

Other devices from Ace Surgical Supply Co., Inc.

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

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
Other properties (12, all answered No)