510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K926036Substantially Equivalent

Acufex Suture Retriever

Acufex Microsurgical, Inc., Mansfield MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K926036 is the FDA 510(k) clearance record for ACUFEX SUTURE RETRIEVER, a class I device, cleared for Acufex Microsurgical, Inc. on under FDA product code GAE (Snare, Surgical). FDA records list 78 510(k) clearances for Acufex Microsurgical, Inc., from to . As of , FDA records show no recalls naming K926036.

Clearance record

Decision date
Received
(155 days to decision)
Product code
GAE Snare, Surgical
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Acufex Microsurgical, Inc. 130 Forbes Blvd., Mansfield MA
510(k) summary
Statement
Third party review
No

Clearances, product code GAE

Trailing 12 months

FDA records hold no clearances under product code GAE in the trailing twelve months.

FDA records show no clearances under product code GAE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GAE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260