Micromedics, Inc. is one of 13389 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, MALLEABLE TIP ENDOSCOPIC APPLICATOR, 360 GAS ASSISTED ENDOSCOPIC APPLICATOR
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.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
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