Identity
- Trade Name
- Lateral Approach Side Cutter FDA UDI
- Generic Name
- Dental mandrel FDA UDI
- Model / Reference
- LASC-7.0 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800041043491 FDA UDI
- FDA Product Code
- NDP FDA UDI
- GMDN Term
- Dental mandrel FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental mandrel
Lateral Approach Side Cutter by Surgident — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental mandrel.
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- Young — YOUNG DENTAL MANUFACTURING I, LLC · Class I
- CEKA & PRECI-LINE ATTACHMENTS — Alpha-Dent · Class I
- CEKA & PRECI-LINE ATTACHMENTS — Alpha-Dent · Class I
- CEKA & PRECI-LINE ATTACHMENTS — Alpha-Dent · 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
- Surgident
Sources (1)
- FDA UDI 20d3ffee-3a59-45f4-aa1b-301cd8c0ede3 32 fields · synced May 31, 2026