Skip to content

Ace 04977501

by Ace Surgical Supply Co., Inc.

Ace 04977501 is a Class I device made by Ace Surgical Supply Co., Inc., listed in FDA GUDID since 10 Oct 2019 (UDI-DI 00614950009619), 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 Number00614950009619 UDI-DI Date10 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  • Withdrawn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
Orthopaedic implant driver
Model / Ref / Catalog
04977501
Primary DI / UDI-DI
00614950009619
FDA product code
HWR
GMDN term
Orthopaedic implant driver
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 17 Millimeter

Related devices

Category: Orthopaedic implant driver

Similar devices in this category

Other devices filed under Orthopaedic implant driver.

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
  • Lot / batch number
Other properties (11, all answered No)