510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K812778Substantially Equivalent

The Telos Equipment

The Telos Co., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812778 is the FDA 510(k) clearance record for THE TELOS EQUIPMENT, a class I device, cleared for The Telos Co. on under FDA product code KQW (Goniometer, Nonpowered). FDA records list 2 510(k) clearances for The Telos Co., from to . As of , FDA records show no recalls naming K812778.

Clearance record

Decision date
Received
(64 days to decision)
Product code
KQW Goniometer, Nonpowered
Regulation
21 CFR 888.1520
Device class
Class I
Review panel
Orthopedic
Applicant
The Telos Co. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code KQW

Trailing 12 months

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

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