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Pmi Pmitcsgxlkt

by Progressive Medical, Inc.

Pmi Pmitcsgxlkt is a Class I device made by Progressive Medical, Inc., listed in FDA GUDID since 13 Mar 2020 (UDI-DI 00812608022076), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00812608022076 UDI-DI Date13 Mar 2020ListedStatusListed 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  • Withdrawn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
Pmi
Generic name
Laparoscopic wound closure thread
Model / reference
PMITCSGXLKT
Primary DI / UDI-DI
00812608022076
FDA product code
KDD
GMDN term
Laparoscopic wound closure thread
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KDD (Kit, Surgical Instrument, Disposable).

Other devices from Progressive Medical, Inc.

See all devices from Progressive Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (6, all answered No)