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LW Fixture

FDA UDI

Class II (US FDA UDI)

by Ossvis Co., Ltd.

Identity

Trade Name
LW Fixture FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Dental Implant Fixture FDA UDI
Model / Reference
LWSF4508SC FDA UDI
Description
Dental Implant Fixture FDA UDI

Identifiers

Primary DI / UDI-DI
08809918230071 FDA UDI
510(k) Number
K223924 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
MRI Safety
MR Conditional FDA UDI

Category: Screw endosteal dental implant, two-piece

LW Fixture 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ossvis Co., Ltd.

Sources (1)

  • FDA UDI f05ee321-7e24-494e-9f17-fea310a2a377 34 fields · synced May 30, 2026