Identity
- Trade Name
- Waterpik Krex Z.O.E. Impression Corrective Paste FDA UDI
- Generic Name
- Dental articulation paste/solution FDA UDI
- Device Name
- Zinc oxide eugenol impression corrective paste, Type II medium-bodied FDA UDI
- Model / Reference
- 015100-000 FDA UDI
- Description
- Zinc oxide eugenol impression corrective paste, Type II medium-bodied FDA UDI
Identifiers
- Catalog Number
- 015100-000 FDA UDI
- Primary DI / UDI-DI
- D686151003 FDA UDI
- FDA Product Code
- EMB FDA UDI
- GMDN Term
- Dental articulation paste/solution FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3275 FDA UDI
- Commercial Distribution
- Not 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
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Weight — 80 Gram FDA UDIWeight — 65 Gram FDA UDI
Waterpik Krex Z.O.E. Impression Corrective Paste by Water Pik, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
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Manufacturer
- Manufacturer
- Water Pik, Inc.
Sources (1)
- FDA UDI 8b595d11-1363-4f21-b52a-74954917b0a9 38 fields · synced May 30, 2026