Summit Medical, Inc. is one of 12957 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Summit Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: InstruSafe(R) Sterilization Container, MINNE TIES MMF Suture System, Instru-Safe Instrument Protection System
9
Total
9
Cleared
0
Denied
Summit Medical, Inc. has 9 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 9 cleared submissions from 2014 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Summit Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Summit Medical, Inc.
9 devices
Cleared
Nov 16, 2018
InstruSafe(R) Sterilization Container
General Hospital
261d
Cleared
Apr 11, 2017
MINNE TIES MMF Suture System
Dental
260d
Cleared
Aug 18, 2015
Instru-Safe Instrument Protection System
General Hospital
109d
Cleared
Jun 22, 2015
Instru-Safe Instrument Protection System
General Hospital
111d
Cleared
May 29, 2015
Instru-Safe Instrument Protection System
General Hospital
246d
Cleared
Dec 23, 2014
Instru-Safe Instrument Protection System
General Hospital
97d
Cleared
Dec 15, 2014
INSTRU-SAFE INSTRUMENT PROTECTION SYSTEM
General Hospital
189d
Cleared
Jun 27, 2014
INSTRU-SAFE INSTRUMENT PROTECTION SYSTEM
General Hospital
142d
Cleared
Mar 13, 2014
INSTRU-SAFE INSTRUMENT PROTECTION SYSTEM
General Hospital
169d