Sds Dental, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sds Dental, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Sds Dental, Inc. has 21 FDA 510(k) cleared dental devices. Based in Washington, US.
Historical record: 21 cleared submissions from 1986 to 1999.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sds Dental, Inc.
21 devices
Cleared
Nov 05, 1999
DELSONIC 2000
Dental
256d
Cleared
Aug 11, 1999
JETSONIC 2000
Dental
170d
Cleared
Jan 22, 1997
DELIVERY SYSTEM(SDS 1400 XL)/DELIVERY SYSTEM CUSPIDOR(SDS1450,SDS1650 XL)
Dental
65d
Cleared
Sep 10, 1990
SURGICAL LIGHTING-CENTRA 450
General & Plastic Surgery
73d
Cleared
Sep 10, 1990
BAUMER SURGICAL TABLE
General & Plastic Surgery
73d
Cleared
Oct 10, 1986
DENTATUS LS/EUROFLEX F-IV/ISOLIGHT REFLECT/CM-II
Dental
63d
Cleared
Oct 01, 1986
EUROFLEX F-IV, ISOFLEX III
Dental
54d
Cleared
Oct 01, 1986
MINILAX SET
Dental
54d
Cleared
Oct 01, 1986
ISOLAX PEDAL SET
Dental
54d
Cleared
Oct 01, 1986
ISOPRAT F-III SET/ISOLAX CHAIR
Dental
54d
Cleared
Oct 01, 1986
ISOPRAT C-III SET/ISOCART III AUXILIARY UNIT
Dental
54d
Cleared
Oct 01, 1986
DENTATUS L SET
Dental
54d
Cleared
Oct 01, 1986
CM-II, CM-I WATER UNIT
Dental
54d
Cleared
Sep 29, 1986
F-11 REFLECTOR / F-II STANDARD REFLECTOR
Dental
52d
Cleared
Sep 26, 1986
EUROCART SR-4, EUROCART M-IV, ISOCART III
Dental
49d
Cleared
Sep 25, 1986
GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEX
Dental
48d
Cleared
Sep 25, 1986
ISOLAX (GNATUS)/ISOLAX PEDAL/MINILAX
Dental
48d
Cleared
Sep 25, 1986
DENTATUS-S / L / LS / (GNATUS)
Dental
48d
Cleared
Sep 25, 1986
CABINET II AUXILIARY UNIT
Dental
48d
Cleared
Sep 25, 1986
SERINGA TRIPLICE S.L.
Dental
48d
Cleared
Sep 24, 1986
-OM WEST 2000 GNATUS CHAIR
Ophthalmic
47d