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
K030507Substantially Equivalent

T.e.a.r. Tech3 Model #44Tt03

Vision Quest Industries, Inc., Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030507 is the FDA 510(k) clearance record for T.E.A.R. TECH3 MODEL #44TT03, a class II device, cleared for Vision Quest Industries, Inc. on under FDA product code IPF (Stimulator, Muscle, Powered). FDA records list 6 510(k) clearances for Vision Quest Industries, Inc., from to . As of , FDA records show no recalls naming K030507.

Clearance record

Decision date
Received
(90 days to decision)
Product code
IPF Stimulator, Muscle, Powered
Regulation
21 CFR 890.5850
Device class
Class II
Review panel
Physical Medicine
Applicant
Vision Quest Industries, Inc. 18011 Mitchell So., Irvine CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IPF

Trailing 12 months
3 clearances under product code IPF in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IPF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20262
July 20260
August 20260
September 20260
October 20260