Steri-Oss, Inc. - FDA 510(k) Cleared Devices
46
Total
46
Cleared
0
Denied
Steri-Oss, Inc. has 46 FDA 510(k) cleared dental devices. Based in Anaheim, US.
Historical record: 46 cleared submissions from 1992 to 1998.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
46 devices
Cleared
Sep 23, 1998
STERI-OSS' IMPROV TEMPORARY DENTAL CEMENT
Dental
75d
Cleared
Mar 16, 1998
REPLACE CYLINDRICAL IMPLANTS
Dental
40d
Cleared
Dec 05, 1997
STERI-OSS 3.25 MM REPLACE(HYDROXYAPATITE-COATED)DENTAL IMPLANT
Dental
86d
Cleared
Dec 05, 1997
STERI-OSS 3.25 MM REPLACE(TITANIUM PLASMA SPRAYED) DENTAL IMPLANT
Dental
86d
Cleared
Nov 26, 1997
STERI-OSS 3.25 MM REPLACE DENTAL IMPLANT SYSTEM
Dental
78d
Cleared
Nov 07, 1997
STERI-OSS UNTIL IMPLANT CEMENT
Dental
88d
Cleared
Jul 03, 1997
BIO-ESTHETIC INDIRECT ABUTMENT
Dental
176d
Cleared
Mar 31, 1997
STERI-OSS TIODIZED SCREW
Dental
125d
Cleared
Mar 05, 1997
REPLACE TITANIUM IMPLANT SYSTEM
Dental
134d
Cleared
Feb 11, 1997
STERI-OSS GOLD ATTACHMENT SYSTEM
Dental
132d
Cleared
Feb 10, 1997
ROUND DENTAL BUR
Dental
62d
Cleared
Nov 14, 1996
STERI-OSS IMPLANTS FOR SINGLE STAGE PLACEMENT
Dental
90d
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