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Ace Lpo-30-Qfl

by Ace Medical Devices Private Limited

Ace Lpo-30-Qfl is a Class II device made by Ace Medical Devices Private Limited, listed in FDA GUDID since 28 Apr 2025 (UDI-DI 08904148102348), 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 Number08904148102348 UDI-DI Date28 Apr 2025ListedStatusListed 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  • Withdrawn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
Endoscopic electrosurgical electrode, bipolar, single-use
Model / reference
LPO-30-QFL
Primary DI / UDI-DI
08904148102348
FDA product code
FAS, GEI
GMDN term
Endoscopic electrosurgical electrode, bipolar, single-use
Device class
Class II
Regulation number
876.4300, 878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic electrosurgical electrode, bipolar, single-use

Similar devices in this category

Other devices filed under Endoscopic electrosurgical electrode, bipolar, single-use.

Other devices from Ace Medical Devices Private Limited

See all devices from Ace Medical Devices Private Limited →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)