Identity
- Trade Name
- Sculpt I.Q. FDA UDI
- Generic Name
- Dental diode laser system FDA UDI
- Device Name
- EasyTip Endo Pack 25 FDA UDI
- Model / Reference
- 6659291G FDA UDI
- Description
- EasyTip Endo Pack 25 FDA UDI
Identifiers
- Catalog Number
- 6659291G FDA UDI
- Primary DI / UDI-DI
- D8076659291G1 FDA UDI
- FDA Product Code
- ILY FDA UDIGEX FDA UDI
- GMDN Term
- Dental diode laser system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5500 FDA UDI878.4810 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Sculpt I.Q. by Dentsply Sirona Orthodontics Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Dentsply Sirona Orthodontics Inc.
Sources (1)
- FDA UDI 7235b21e-7c1e-4399-ba0a-d860f55e36ae 36 fields · synced Jun 9, 2026