Identity
- Trade Name
- Ortho Pro FDA UDI
- Generic Name
- Orthodontic appliance relief material FDA UDI
- Device Name
- Patient Relief Wax Orange 50pcs/pk FDA UDI
- Model / Reference
- WAX-OR FDA UDI
- Description
- Patient Relief Wax Orange 50pcs/pk FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810152825921 FDA UDI
- FDA Product Code
- EGD FDA UDI
- GMDN Term
- Orthodontic appliance relief material FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6890 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Orthodontic appliance relief material
Ortho Pro by Ortho Pro Dent LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthodontic appliance relief material.
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- Gishy Goo — ULTRADENT PRODUCTS, INC. · Class I
- PATIENT RELIEF WAX — Ortho Organizers, Inc. · Class I
- JMU — JMU DENTAL, INC · Class I
- Ortho Organizers — Ortho Organizers, Inc. · Class I
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
- Ortho Pro Dent LLC
Sources (1)
- FDA UDI f330fd44-af6f-426e-95f3-8caffdcfe4b9 35 fields · synced Jun 6, 2026