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FatSilk 19-7500

by Innovative Med, Inc.

FatSilk 19-7500 is a Class I device made by Innovative Med, Inc., listed in FDA GUDID since 26 Jun 2019 (UDI-DI 00851314007380), 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 Number00851314007380 UDI-DI Date26 Jun 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  • Withdrawn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
FatSilk
Generic name
Suction system filter, tissue, sterile
Model / reference
19-7500
Primary DI / UDI-DI
00851314007380
FDA product code
KET
GMDN term
Suction system filter, tissue, sterile
Device class
Class I
Regulation number
864.3010
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KET (Filters, Cell Collection, Tissue Processing).

Other devices from Innovative Med, Inc.

See all devices from Innovative Med, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)