510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K936311Substantially Equivalent for Some Indications

Mitek Mini Anchor

Mitek Surgical Products, Inc., Norwood MA / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K936311 is the FDA 510(k) clearance record for MITEK MINI ANCHOR, a class II device, cleared for Mitek Surgical Products, Inc. on under FDA product code MNV (Strip, Dialysate Ph Indicator). FDA records list 31 510(k) clearances for Mitek Surgical Products, Inc., from to . As of , FDA records show no recalls naming K936311.

Clearance record

Decision date
Received
(559 days to decision)
Product code
MNV Strip, Dialysate Ph Indicator
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Mitek Surgical Products, Inc. 57 Providence Hwy., Norwood MA
Third party review
No

Clearances, product code MNV

Trailing 12 months

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

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