Identity
- Trade Name
- Facial Plane Relator FDA UDI
- Generic Name
- Facebow FDA UDI
- Device Name
- This product can be used with bite registration material.The horizontal alignment bar features an arch with 25 fingers for stabilizing the unit within the registration material. The vertical alignment bar snaps on. Comes in bulk of 100 FDA UDI
- Model / Reference
- FPR-102 FDA UDI
- Description
- This product can be used with bite registration material.The horizontal alignment bar features an arch with 25 fingers for stabilizing the unit within the registration material. The vertical alignment bar snaps on. Comes in bulk of 100 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850211006144 FDA UDI
- FDA Product Code
- KCR FDA UDI
- GMDN Term
- Facebow FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3220 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Facebow
Facial Plane Relator by Ho Dental Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Ho Dental Co., Inc.
Sources (1)
- FDA UDI 9e0d1b47-ce00-4e92-b802-d45a1a33b22a 33 fields · synced Jun 6, 2026