510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K092675Substantially Equivalent

Grindcare

Medotech A/S, Westminster CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K092675 is the FDA 510(k) clearance record for GRINDCARE, a class II device, cleared for Medotech A/S on under FDA product code HCC (Device, Biofeedback). FDA records list 2 510(k) clearances for Medotech A/S, from to . As of , FDA records show no recalls naming K092675.

Clearance record

Decision date
Received
(183 days to decision)
Product code
HCC Device, Biofeedback
Regulation
21 CFR 882.5050
Device class
Class II
Review panel
Neurology
Applicant
Medotech A/S 13417 Quivas St., Westminster CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HCC

Trailing 12 months

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

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