510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K032238Substantially Equivalent

Twister Superelastic Ligating Clip and Applier

Neurosel (Medical) Limited, Andover, Hampshire, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K032238 is the FDA 510(k) clearance record for TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER, a class II device, cleared for Neurosel (Medical) Limited on under FDA product code FZP (Clip, Implantable). FDA records list one 510(k) clearance for Neurosel (Medical) Limited. As of , FDA records show no recalls naming K032238.

Clearance record

Decision date
Received
(50 days to decision)
Product code
FZP Clip, Implantable
Regulation
21 CFR 878.4300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Neurosel (Medical) Limited Greenways, Andover, Hampshire, GB
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