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Ace 03605001

by Ace Surgical Supply Co., Inc.

Ace 03605001 is a Class II device made by Ace Surgical Supply Co., Inc., listed in FDA GUDID since 19 Oct 2019 (UDI-DI 00614950021512), 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 Number00614950021512 UDI-DI Date19 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  • Withdrawn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 prosthesis/implant abutment screw analog, single-use
Model / Ref / Catalog
03605001
Description
* IMPRESSION COPING PLUGS DELRIN 5/PKG
Primary DI / UDI-DI
00614950021512
FDA product code
DZE
GMDN term
Dental prosthesis/implant abutment screw analog, single-use
Device class
Class II
Regulation number
872.3640
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Ace Surgical Supply Co., Inc.

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

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)