Skip to content

Edgetec Edge-3.2A

by Unique Technologies, Inc.

Edgetec Edge-3.2A is a Class I device made by Unique Technologies, Inc., listed in FDA GUDID since 1 Sep 2023 (UDI-DI 00840120302994), 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 Number00840120302994 UDI-DI Date1 Sep 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  • Withdrawn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
Edgetec
Generic name
Scalpel, single-use
Model / reference
EDGE-3.2A
Primary DI / UDI-DI
00840120302994
FDA product code
HNN
GMDN term
Scalpel, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Scalpel, single-use

Similar devices in this category

Other devices filed under Scalpel, single-use.

Other devices from Unique Technologies, Inc.

See all devices from Unique Technologies, Inc. →

Properties

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