Medical Device Manufacturer · US , Washington , DC

Specialites Septodont - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1985

21

Total

21

Cleared

0

Denied

FDA 510(k) Regulatory Record - Specialites Septodont Dental ✕

19 devices

1-19 of 19

Cleared Oct 09, 2001

PHARMAETHYL LOCAL PULP AND VITALITY TESTING AGENT

Cleared Jul 23, 2001

Cleared Nov 03, 1998

QUICKSET LIQUID AND POWDER

Cleared Oct 19, 1998

Cleared May 01, 1998

Cleared Apr 21, 1992

SEPTOCALCINE ULTRA

Cleared Feb 03, 1992

SEPTOPACK TEMPORARY FILLING

Cleared Feb 03, 1992

CIMPAT S DENTAL CEMENT

Cleared Nov 07, 1991

SAFETY PLUS DENTAL INJECTION NEEDLE

Cleared Oct 09, 1991

AUTOPACK NON-EUGENOL PERIODONTAL DRESSING

Cleared Sep 30, 1991

SEPTOCAL CAVITY LINER

Cleared Jul 09, 1990

CYANODONT DENTAL CEMENT

Cleared Dec 21, 1989

SILCOT COPAL CAVITY VARNISH

Cleared Mar 01, 1989

CIMPAT S TEMPORARY DENTAL CEMENT

Cleared Jan 19, 1989

Cleared Jul 15, 1988

PROVISCEM OR PROVISCELL EUGENOL-FREE DENTAL CEMENT

Cleared Jun 07, 1988

IONOSCEM OR IONOSCELL GLASS IONOMER DENTAL CEMENT

Cleared Sep 23, 1985

SEPTOJECT STERILE DISPOSABLE INJECTION NEEDLE

Cleared May 29, 1985

SEPTOSIL SILICONE FOR PRECISION IMPRESSION