510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925335Substantially Equivalent

Acufex Intra Articular Measuring Device

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

K925335 is the FDA 510(k) clearance record for ACUFEX INTRA ARTICULAR MEASURING DEVICE, a class I device, cleared for Acufex Microsurgical, Inc. on under FDA product code HTJ (Gauge, Depth). FDA records list 78 510(k) clearances for Acufex Microsurgical, Inc., from to . As of , FDA records show no recalls naming K925335.

Clearance record

Decision date
Received
(68 days to decision)
Product code
HTJ Gauge, Depth
Regulation
21 CFR 888.4300
Device class
Class I
Review panel
Orthopedic
Applicant
Acufex Microsurgical, Inc. 130 Forbes Blvd., Mansfield MA
510(k) summary
Statement
Third party review
No

Clearances, product code HTJ

Trailing 12 months

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

FDA records show no clearances under product code HTJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HTJ, 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