Pulpdent Corporation 80 Oakland Street, Watertown, MA 02472, USA
Philippines9 devices1 country
VerifiedFDA Philippines · official registry
9
Total Devices
1
Countries
2024
Earliest
2025
Latest
Regulatory footprint
Search Pulpdent Corporation 80 Oakland Street, Watertown, MA 02472, USA across other regulatory registries
Recent registrations
Latest 10 FDA device registrations
Pulpdent® Periocare™ Periodontal Dressing
May 06, 2025
- Registration
- CMDR-2025-04522
- Country
- USA
Surgicom Trading Corp.
May 24, 2024
- Registration
- MDR-06662
- Country
- USA
Pulpdent® Dentin Conditioning Gel™ 22% Polyacrylic Acid
May 08, 2024
- Registration
- CMDR-2024-02803
- Country
- USA
PULPDENT® BIOACTIVE - BASE/LINER™ Dental Base/Liner
May 06, 2024
- Registration
- MDR-06639
- Country
- USA
Pulpdent® Seal-Rite™ Pit and Fissure Sealant
Mar 08, 2024
- Registration
- MDR-04854
- Country
- USA
Pulpdent® Lime-Lite™ Enhanced Light Cure Cavity Liner
Mar 04, 2024
- Registration
- CMDR-2024-02404
- Country
- USA
Pulpdent® Porcelain Etch Gel (9.6% Hydroflouric Acid)
Mar 04, 2024
- Registration
- CMDR-2024-02403
- Country
- USA
Pulpdent Multi-Cal Calcium Hydroxide Preparation (paste)
Mar 04, 2024
- Registration
- CMDR-2024-02400
- Country
- USA
PULPDENT FORENDO Paste Calcium Hydroxide with Iodoform Root Canal Treatment Paste
Jan 30, 2024
- Registration
- CMDR-2024-02323
- Country
- USA
Country distribution
Devices by country of origin
USA9100.0% of total
About this profile
Explore comprehensive manufacturer profile for Pulpdent Corporation 80 Oakland Street, Watertown, MA 02472, USA through Pure Global AI's free Philippines medical device database. This company manufactures 9 medical devices registered with FDA from 1 country. Their registration history spans from Jan 30, 2024 to May 06, 2025.
This page provides detailed insights including recent registrations, country distribution (USA: 9), and complete regulatory information from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry.