510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K862286Substantially Equivalent

Arthrophonometer

Arthrotek, Inc., West Hartford CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862286 is the FDA 510(k) clearance record for ARTHROPHONOMETER, a class I device, cleared for Arthrotek, Inc. on under FDA product code NFQ (Device, Dental Sonography, For Monitoring Jaw Sounds). FDA records list 17 510(k) clearances for Arthrotek, Inc., from to . As of , FDA records show no recalls naming K862286.

Clearance record

Decision date
Received
(205 days to decision)
Product code
NFQ Device, Dental Sonography, For Monitoring Jaw Sounds
Regulation
21 CFR 872.2050
Device class
Class I
Review panel
Dental
Applicant
Arthrotek, Inc. 30 Sherman St., West Hartford CT
Third party review
No

Clearances, product code NFQ

Trailing 12 months

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

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