Identity
- Trade Name
- AnyOne Onestage Fixture FDA UDI
- Generic Name
- Screw endosteal dental implant, two-piece FDA UDI
- Device Name
- Ø4/ L=8.5/ C=1.8 FDA UDI
- Model / Reference
- OSF4008 FDA UDI
- Description
- Ø4/ L=8.5/ C=1.8 FDA UDI
Identifiers
- Catalog Number
- OSF4008H FDA UDI
- Primary DI / UDI-DI
- 08806388246632 FDA UDI
- 510(k) Number
- K210161 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Screw endosteal dental implant, two-piece
AnyOne Onestage Fixture by Megagen Implant Co. Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Screw endosteal dental implant, two-piece.
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Cleared under the same submission
K210161 also covers:
- Abutment Screw — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant Co. Ltd
- AnyOne Onestage Fixture — Megagen Implant 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 |
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Manufacturer
- Manufacturer
- Megagen Implant Co. Ltd
Sources (1)
- FDA UDI be80c05a-7b0b-4863-8482-72fd57a5cb94 35 fields · synced May 30, 2026