Identity
- Trade Name
- Solid Abutment FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- AnyOne Internal Ø4/ C=4.5/ P=5.5 FDA UDI
- Model / Reference
- SL40455 FDA UDI
- Description
- AnyOne Internal Ø4/ C=4.5/ P=5.5 FDA UDI
Identifiers
- Catalog Number
- SL40455 FDA UDI
- Primary DI / UDI-DI
- 08806388235964 FDA UDI
- 510(k) Number
- K123988 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental implant suprastructure, permanent, preformed
Solid Abutment by Megagen Implant Co. Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental implant suprastructure, permanent, preformed.
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Cleared under the same submission
K123988 also covers:
- Angled Abutment — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal Fixture — Megagen Implant Co. Ltd
- AnyOne Internal 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 75a84f12-a167-4114-b845-e2fd27e689df 35 fields · synced Jun 6, 2026