510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K091060Substantially Equivalent

Vesocclude Ligating Clip

Vesocclude Medical, LLC, Spring Hope NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K091060 is the FDA 510(k) clearance record for VESOCCLUDE LIGATING CLIP, a class II device, cleared for Vesocclude Medical, LLC on under FDA product code FZP (Clip, Implantable). FDA records list 2 510(k) clearances for Vesocclude Medical, LLC, from to . As of , FDA records show no recalls naming K091060.

Clearance record

Decision date
Received
(162 days to decision)
Product code
FZP Clip, Implantable
Regulation
21 CFR 878.4300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Vesocclude Medical, LLC 10419 Stallings Rd., Spring Hope NC
510(k) summary
Summary PDF
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