Impladent , Ltd. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Impladent , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Impladent , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Hollis, US.
Historical record: 5 cleared submissions from 1996 to 2014. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Impladent , Ltd. Filter by specialty or product code using the sidebar.
Impladent , Ltd. — FDA 510(k) Products and Clearance History
5 devices
Cleared
Dec 18, 2014
TRISTAR BONE GRAFT FIXATION SYSTEM
Dental
170d
Cleared
Dec 10, 2009
OSTEOTAPE
Dental
261d
Cleared
Apr 27, 2004
OSTEOGEN SBRG
Dental
211d
Cleared
May 18, 1999
LAMINOSS DENTAL IMPLANT
Dental
271d
Cleared
Jun 24, 1996
LAMINOSS DENTAL IMPLANT
Dental
1060d