Not currently registered with FDA under this name
Pulpdent Corp. of America
Brookline, MA, United States. Named as applicant on 5 dental 510(k) clearances between 1981 and 1988. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 51981–1988
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1980–2026
510(k) clearances
Clearances on which FDA names Pulpdent Corp. of America as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 15 Jul 1988 | K882576 | ACID ETCH GEL | EBF Resin Tooth Shade Material |
| 20 Feb 1986 | K854977 | FIBER MESH | DZE Root-Form Endosseous Implant |
| 29 Oct 1985 | K844446 | BISICO SL(PUTTY) BISICO S2(REGULAR) S3 HEAVY ETC. | ELW Impression Material |
| 16 Oct 1985 | K853447 | POLYCARB WATER SET | EMA Dental Cement |
| 24 Mar 1981 | K810545 | PCA PERIOCARE PERIODONTAL DRESSING | EMA Dental Cement |
Some of these clearances are listed with FDA today by another company: Pulpdent Corporation (3), Zest Anchors, LLC (1).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.