Micromedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Micromedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Endoscopic Applicator, 41 cm
29
Total
29
Cleared
0
Denied
Micromedics, Inc. has 29 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Latest FDA clearance: Jul 2024. Active since 1983.
Browse the FDA 510(k) cleared devices submitted by Micromedics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Micromedics, Inc.
29 devices
Cleared
Jul 15, 2024
Endoscopic Applicator, 41 cm
General & Plastic Surgery
28d
Cleared
Jan 08, 2013
MALLEABLE TIP ENDOSCOPIC APPLICATOR
General & Plastic Surgery
25d
Cleared
Nov 16, 2012
360 GAS ASSISTED ENDOSCOPIC APPLICATOR
General & Plastic Surgery
88d
Cleared
Mar 15, 2012
ENDOSCOPIC APPLICATOR
General & Plastic Surgery
15d
Cleared
Mar 15, 2011
SINGLE CANNULA EXTENDED APPLICATOR
General Hospital
189d
Cleared
Jun 09, 2010
GRAFT DELIVERY SYSTEM MODEL SA-6115
General Hospital
84d
Cleared
Mar 14, 2008
EARPOPPER, MODEL EP-2000, EP-2100, EP-3000
Ear, Nose, Throat
101d
Cleared
Sep 13, 2006
BAXTER DUPLOSPRAY MIS APPLICATOR
General Hospital
147d
Cleared
Sep 01, 2005
INSTRU-SAFE INSTRUMENT PROTECTION SYSTEMS
General Hospital
119d
Cleared
Apr 27, 2005
MICROMEDICS SPHENOID SINUS STENT
General & Plastic Surgery
75d
Cleared
Feb 11, 2005
MICROMEDICS FIBRIJET AIR ASSISTED ENDOSCOPIC APPLICATOR
General & Plastic Surgery
121d
Cleared
Oct 04, 2004
BAXTER DUPLOTIP SURGICAL SEALANT APPLICATOR
General Hospital
326d