Identity
- Trade Name
- 20:1 CONTRA ANGLE FDA UDI
- Generic Name
- Dental power tool system handpiece, line-powered FDA UDI
- Model / Reference
- LCC-120A FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04719873120666 FDA UDI
- 510(k) Number
- K162856 FDA UDI
- FDA Product Code
- EGS FDA UDI
- GMDN Term
- Dental power tool system handpiece, line-powered FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4200 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental power tool system handpiece, line-powered
20:1 Contra Angle by Bonart Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental power tool system handpiece, line-powered.
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- MEDIDENTA — HANDPIECE PARTS & REPAIRS, INC. · Class I
- SM3 — Osstem Implant Co., Ltd._Gasan Branch · Class II
- Delfin — Intra-Lock International · Class I
- EXPERTmatic E15 L — KaVo Dental GmbH · Class I
Cleared under the same submission
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
- Bonart Co., Ltd.
Sources (1)
- FDA UDI 14e58fa3-a6a4-4e15-910c-49ad6a4f4441 33 fields · synced Jun 8, 2026