Medical Device Manufacturer · US , Washington , DC

Sds Dental, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1986

21

Total

21

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sds Dental, Inc. Dental ✕

18 devices

1-18 of 18

Cleared Nov 05, 1999

Cleared Aug 11, 1999

Cleared Jan 22, 1997

DELIVERY SYSTEM(SDS 1400 XL)/DELIVERY SYSTEM CUSPIDOR(SDS1450,SDS1650 XL)

Cleared Oct 10, 1986

DENTATUS LS/EUROFLEX F-IV/ISOLIGHT REFLECT/CM-II

Cleared Oct 01, 1986

EUROFLEX F-IV, ISOFLEX III

Cleared Oct 01, 1986

Cleared Oct 01, 1986

ISOLAX PEDAL SET

Cleared Oct 01, 1986

ISOPRAT F-III SET/ISOLAX CHAIR

Cleared Oct 01, 1986

ISOPRAT C-III SET/ISOCART III AUXILIARY UNIT

Cleared Oct 01, 1986

Cleared Oct 01, 1986

CM-II, CM-I WATER UNIT

Cleared Sep 29, 1986

F-11 REFLECTOR / F-II STANDARD REFLECTOR

Cleared Sep 26, 1986

EUROCART SR-4, EUROCART M-IV, ISOCART III

Cleared Sep 25, 1986

GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEX

Cleared Sep 25, 1986

ISOLAX (GNATUS)/ISOLAX PEDAL/MINILAX

Cleared Sep 25, 1986

DENTATUS-S / L / LS / (GNATUS)

Cleared Sep 25, 1986

CABINET II AUXILIARY UNIT

Cleared Sep 25, 1986

SERINGA TRIPLICE S.L.