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
K901305Substantially Equivalent

Model 2121-21, Tmj Surface Coil

Medical Advances, Inc., Milwaukee WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901305 is the FDA 510(k) clearance record for MODEL 2121-21, TMJ SURFACE COIL, a class II device, cleared for Medical Advances, Inc. on under FDA product code LNH (System, Nuclear Magnetic Resonance Imaging). FDA records list 57 510(k) clearances for Medical Advances, Inc., from to . As of , FDA records show no recalls naming K901305.

Clearance record

Decision date
Received
(37 days to decision)
Product code
LNH System, Nuclear Magnetic Resonance Imaging
Regulation
21 CFR 892.1000
Device class
Class II
Review panel
Radiology
Applicant
Medical Advances, Inc. 10431 W. Watertown Plank Rd., Milwaukee WI
Third party review
No

Clearances, product code LNH

Trailing 12 months
25 clearances under product code LNH in the twelve months to October 2026, March 2026 the highest month at 6.
Show the numbers
Monthly 510(k) clearances under FDA product code LNH, trailing twelve months
MonthClearances
November 20251
December 20253
January 20261
February 20264
March 20266
April 20261
May 20261
June 20260
July 20262
August 20263
September 20263
October 20260