Identity
- Trade Name
- PANAVIA™ 21 FDA UDI
- Generic Name
- Dental composite resin kit FDA UDI
- Device Name
- DISPENSER FDA UDI
- Model / Reference
- #930-KA FDA UDI
- Description
- DISPENSER FDA UDI
Identifiers
- Primary DI / UDI-DI
- EKUR000930KA1 FDA UDI
- 510(k) Number
- K012438 FDA UDI
- FDA Product Code
- EMA FDA UDI
- GMDN Term
- Dental composite resin kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3275 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental composite resin kit
Panavia™ 21 by Kuraray Noritake Dental Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K012438 also covers:
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
- PANAVIA™ 21 — KURARAY NORITAKE DENTAL INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Kuraray Noritake Dental Inc.
Sources (1)
- FDA UDI 4e7bca6e-2e2f-46f9-838c-fdc99872d038 34 fields · synced May 29, 2026