Identifiers
- 510(k) Number
- K993545 FDA 510(k)
- FDA Product Code
- ELR FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 872.3810 FDA 510(k)
- Regulation Number
- 872.3810 FDA 510(k)
- Advisory Committee
- Dental FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Tenax White Post by Coltene/Whaledent Inc. — Class I — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K993545 | Class I | Active |
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Manufacturer
- Manufacturer
- Coltene/Whaledent Inc.
- FDA Applicant
- Coltene/Whaledent, Inc.
Sources (1)
- FDA 510(k) K993545 24 fields · synced Jun 18, 2026