Identity
- Trade Name
- Masel FDA UDI
- Generic Name
- Interproximal reduction kit FDA UDI
- Device Name
- LIGHTINING STRIPS DOUBLE-SIDED X-WIDE FDA UDI
- Model / Reference
- 2035-050 FDA UDI
- Description
- LIGHTINING STRIPS DOUBLE-SIDED X-WIDE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00190707041465 FDA UDI
- FDA Product Code
- EHM FDA UDI
- GMDN Term
- Interproximal reduction kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6010 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
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
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: Interproximal reduction kit
Masel by Ortho Organizers, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Interproximal reduction kit.
- SureSmile® — Dentsply Sirona Orthodontics Inc. · Class I
- IPR Lamineer Tips — Dentatus AB · Class I
- MICROCUT — TDV DENTAL LTDA · Class I
- IPR Lamineer Tips — Dentatus AB · Class I
- MICROCUT — TDV DENTAL LTDA · Class I
- Profin with IPR Lamineer Tips — Dentatus AB · Class I
- MICROCUT — TDV DENTAL LTDA · Class I
- IPR Lamineer Tips — Dentatus AB · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ortho Organizers, Inc.
Sources (1)
- FDA UDI 935880a9-3d4a-43c7-978d-b7e871b14131 33 fields · synced Jun 9, 2026