510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K911915Substantially Equivalent

Hemoclip II

Edward Weck, Inc., Research Triangle Pa NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K911915 is the FDA 510(k) clearance record for HEMOCLIP II, a class II device, cleared for Edward Weck, Inc. on under FDA product code FZP (Clip, Implantable). FDA records list 140 510(k) clearances for Edward Weck, Inc., from to . As of , FDA records show no recalls naming K911915.

Clearance record

Decision date
Received
(254 days to decision)
Product code
FZP Clip, Implantable
Regulation
21 CFR 878.4300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Edward Weck, Inc. P.O. Box 12600, Research Triangle Pa NC
510(k) summary
Statement
Third party review
No

Clearances, product code FZP

Trailing 12 months
5 clearances under product code FZP in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FZP, trailing twelve months
MonthClearances
November 20251
December 20252
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20261
October 20260