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Bluediamond Implant

FDA UDI

Class II (US FDA UDI)

by Megagen Implant Co. Ltd

Identity

Trade Name
BLUEDIAMOND IMPLANT FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Ø4.8x5.0 FDA UDI
Model / Reference
BDC480502 FDA UDI
Description
Ø4.8x5.0 FDA UDI

Identifiers

Catalog Number
BDC480502C FDA UDI
Primary DI / UDI-DI
08809985666391 FDA UDI
510(k) Number
K241972 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

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
MRI Safety
MR Conditional FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Bluediamond Implant by Megagen Implant Co. Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd5d96fe-03b6-4221-a7de-d7e8511cf200 35 fields · synced Jun 1, 2026