Is this your brand? Sign in to claim ownership.
Sign in to claim this brandDHARMA RESEARCH, INC.
US
Last updated May 27, 2026
Information
- Country
- US
- Address
- —
- Website
- dharmaresearch.com
- —
- —
- [email protected]
- Phone
- 8778333725
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 078444642
Catalogue (28)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Enthus | 38-00004 | FDA UDI | Class II | Active |
| Citrine | 56-00202 | FDA UDI | Class II | Active |
| Jade | 20-00016 | FDA UDI | Class II | Active |
| Enthus | 38-00010 | FDA UDI | Class II | Active |
| Jade | 20-00009 | FDA UDI | Class II | Active |
| Jade | 20-00010 | FDA UDI | Class II | Active |
| Enthus | 38-00007 | FDA UDI | Class II | Active |
| Jade | 20-00007 | FDA UDI | Class II | Active |
| Jade | 20-00005 | FDA UDI | Class II | Active |
| Enthus | 38-00009 | FDA UDI | Class II | Active |
| Enthus | 38-00002 | FDA UDI | Class II | Active |
| Jade | 20-00008 | FDA UDI | Class II | Active |
| Jade | 20-00006 | FDA UDI | Class II | Active |
| Enthus | 38-00005 | FDA UDI | Class II | Active |
| Jade | 20-00003 | FDA UDI | Class II | Active |
| Enthus | 38-00012 | FDA UDI | Class II | Active |
| Enthus | 38-00001 | FDA UDI | Class II | Active |
| Enthus | 38-00011 | FDA UDI | Class II | Active |
| Enthus | 38-00003 | FDA UDI | Class II | Active |
| Jade | 20-00004 | FDA UDI | Class II | Active |
| Citrine | 56-00200 | FDA UDI | Class II | Active |
| Enthus | 38-00006 | FDA UDI | Class II | Active |
| Jade | 20-00001 | FDA UDI | Class II | Active |
| Jade | 20-00002 | FDA UDI | Class II | Active |
| Jade | 20-00091 | FDA UDI | Class II | Active |
| Citrine | 56-00204 | FDA UDI | Class II | Active |
| Enthus | 38-00008 | FDA UDI | Class II | Active |
| Jade 37% Phosphoric Acid Etchant Gel | K150696 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Sep 29, 2014 | Z-0476-2015 | — | terminated | During an FDA inspection it was found that the products are marketed without a cleared 510k. |
| Sep 29, 2014 | Z-0475-2015 | — | terminated | During an FDA inspection, it was found that the products are being marketed without a cleared 510k. |