Identity
- Trade Name
- LW Narrow Implant SLA FDA UDI
- Generic Name
- Screw endosteal dental implant, two-piece FDA UDI
- Device Name
- Submerged Dental Implant FDA UDI
- Model / Reference
- LWNF3511S FDA UDI
- Description
- Submerged Dental Implant FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809918249882 FDA UDI
- 510(k) Number
- K233808 FDA UDI
- FDA Product Code
- DZE FDA UDI
- GMDN Term
- Screw endosteal dental implant, two-piece FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3640 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
MR Conditional FDA UDI
Category: Screw endosteal dental implant, two-piece
LW Narrow Implant SLA by Ossvis Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Screw endosteal dental implant, two-piece.
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- ET II Fixture SA Mini No-Mounted — HIOSSEN INC. · Class II
- PRAMA RF WHITE IMPLANT ZIRTI — SWEDEN & MARTINA INC · Class II
- UF(II) Wide — DIO Corporation · Class II
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Cleared under the same submission
K233808 also covers:
- LW Narrow Cover Screw — Ossvis Co., Ltd.
- LW Narrow Cover Screw — Ossvis Co., Ltd.
- LW Narrow Cover Screw — Ossvis Co., Ltd.
- LW Narrow Healing Abutment — Ossvis Co., Ltd.
- LW Narrow Healing Abutment — Ossvis Co., Ltd.
- LW Narrow Healing Abutment — Ossvis Co., Ltd.
- LW Narrow Healing Abutment — Ossvis Co., Ltd.
- LW Narrow Healing Abutment — Ossvis Co., Ltd.
- LW Narrow Healing Abutment — Ossvis Co., Ltd.
- LW Narrow Implant — Ossvis Co., Ltd.
- LW Narrow Implant — Ossvis Co., Ltd.
- LW Narrow Implant SLA — Ossvis Co., Ltd.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ossvis Co., Ltd.
Sources (1)
- FDA UDI bdfbdcd8-e815-40ac-9a4f-1eb6c815cb46 34 fields · synced May 30, 2026