510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K090341Substantially Equivalent

Michigan Cranial Reshaping Orthosis

Danmar Products, Inc., Dearborn MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K090341 is the FDA 510(k) clearance record for MICHIGAN CRANIAL RESHAPING ORTHOSIS, a class II device, cleared for Danmar Products, Inc. on under FDA product code MVA (Orthosis, Cranial). FDA records list 3 510(k) clearances for Danmar Products, Inc., from to . As of , FDA records show no recalls naming K090341.

Clearance record

Decision date
Received
(330 days to decision)
Product code
MVA Orthosis, Cranial
Regulation
21 CFR 882.5970
Device class
Class II
Review panel
Neurology
Applicant
Danmar Products, Inc. 537 Fort Dearborn St., Dearborn MI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MVA

Trailing 12 months

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

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