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K2 Zirkon Blank white classic - K2 Blanks extreme translucent
FDA 510(k)Class II (US FDA 510(k))
510(k) K173971
Identifiers
- 510(k) Number
- K173971 FDA 510(k)
- FDA Product Code
- EIH FDA 510(k)
- Models / Variants
- K2 Zirkon Blank white classic FDA 510(k)K2 Zirkon Blank translucent FDA 510(k)K2 Blanks extreme translucent FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 872.6660 FDA 510(k)
- Regulation Number
- 872.6660 FDA 510(k)
- Advisory Committee
- Dental FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
K2 Zirkon Blank white classic - K2 Blanks extreme translucent by Yeti Dentalprodukte Gmbh — Class II — FDA_510K — listed in FDA 510(k) — 3 models
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 | K173971 | Class II | Active |
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Manufacturer
- Manufacturer
- Yeti Dentalprodukte Gmbh
Sources (1)
- FDA 510(k) K173971 24 fields · synced Jun 18, 2026