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AnyOne Internal Fixture

FDA UDI

Class II (US FDA UDI)

by Megagen Implant Co. Ltd

Identity

Trade Name
AnyOne Internal Fixture FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
AnyOne Internal Ø6/ L=7/ B=2 FDA UDI
Model / Reference
IF6007S FDA UDI
Description
AnyOne Internal Ø6/ L=7/ B=2 FDA UDI

Identifiers

Catalog Number
IF6007SC FDA UDI
Primary DI / UDI-DI
08806388221240 FDA UDI
510(k) Number
K123988 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 Internal Fixture by Megagen Implant 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.

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 0c0cd0cc-180d-4571-b1d4-8898801d0f13 35 fields · synced May 30, 2026