Skip to content

Uterine Manipulator 003276

by Medgyn Products, Inc.

Uterine Manipulator 003276 is an uterine manipulator (FDA Class II; FDA product code LKF, Cannula, Manipulator/Injector, Uterine) made by Medgyn Products, Inc., listed in FDA GUDID since 29 Oct 2026 (UDI-DI 00810072449726), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810072449726 UDI-DI Date29 Oct 2026ListedStatusListed 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  • Withdrawn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
Uterine Manipulator
Generic name
Uterine manipulator, single-use
Model / reference
003276
Primary DI / UDI-DI
00810072449726
FDA product code
LKF
GMDN term
Uterine manipulator, single-use
Device class
Class II
Regulation number
884.4530
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Similar devices

Other devices filed under FDA product code LKF (Cannula, Manipulator/Injector, Uterine).

Other devices from Medgyn Products, Inc.

See all devices from Medgyn Products, Inc. →

Properties

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