Medical Device Manufacturer · US , Washington , DC

Specialites Septodont - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1985

Total

Cleared

Denied

Specialites Septodont has 21 FDA 510(k) cleared dental devices. Based in Washington, US.

Historical record: 21 cleared submissions from 1985 to 2001.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Specialites Septodont is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Specialites Septodont

21 devices

1-12 of 21

Cleared Oct 09, 2001

PHARMAETHYL LOCAL PULP AND VITALITY TESTING AGENT

QUICKSET LIQUID AND POWDER

SEPTOPACK TEMPORARY FILLING

K915466 · EBG

Dental · 60d

Cleared Feb 03, 1992

CIMPAT S DENTAL CEMENT

K915467 · EMA

Dental · 60d

Cleared Nov 07, 1991

SAFETY PLUS DENTAL INJECTION NEEDLE

K913573 · DZM

Dental · 87d

Cleared Oct 09, 1991

AUTOPACK NON-EUGENOL PERIODONTAL DRESSING

K913572 · EMA

Dental · 58d

Cleared Sep 30, 1991

SEPTOCAL CAVITY LINER

General Hospital · 40d

Specialites Septodont - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Specialites Septodont

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