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Hemoclip FTL-HC-09-230-O

by Yangzhou Fartley Medical Instrument Technology Co., Ltd

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06936603227718 UDI-DI Date26 Jan 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Hemoclip
Generic Name
Gastrointestinal endoscopic clip, long-term, non-bioabsorbable
Model / Ref / Catalog
FTL-HC-09-230-O, MMC-230-09
Primary DI / UDI-DI
06936603227718
510(k) Number
FDA Product Code
PKL
GMDN Term
Gastrointestinal endoscopic clip, long-term, non-bioabsorbable
Device Class
Class II
Regulation Number
876.4400
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Cleared under the same submission (K230004)

Other devices from Yangzhou Fartley Medical Instrument Technology Co., Ltd

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No