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Ossvis Co., Ltd.

US

Last updated May 23, 2026

What Ossvis Co., Ltd. makes

Ossvis Co., Ltd. manufactures dental implants and related components, including screw endosteal implants (both one-piece and two-piece designs), temporary preformed suprastructures, and reusable surgical tools like drill bits and screwdrivers. Their portfolio also includes intraoral-scanning abutment analogs, reusable surgical procedure kits, and depth/angle gauges for dental implantation procedures.

The company’s products are regulated under FDA’s Class I and Class II device classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. Ossvis Co., Ltd. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Ossvis Co., Ltd. manufacture?

Ossvis Co., Ltd. specializes in dental implants and associated components. Their portfolio includes screw endosteal dental implants (available as one-piece or two-piece designs), temporary preformed suprastructures for implants, reusable surgical tools like drill bits and screwdrivers, intraoral-scanning abutment analogs, and reusable surgical procedure kits. They also produce dental implantation depth and angle gauges to assist in precise surgical placement.

Where is Ossvis Co., Ltd. based?

Ossvis Co., Ltd. is headquartered in the United States. This location influences their regulatory compliance framework, particularly under FDA guidelines, which govern their product classifications and listing requirements.

Which regulatory registries or databases list Ossvis Co., Ltd.’s devices?

Ossvis Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for their products, which are classified under FDA’s Class I and Class II categories depending on their intended use and risk level.

How are Ossvis Co., Ltd.’s devices classified by regulatory authorities?

Ossvis Co., Ltd.’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
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LinkedIn
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Facebook
—
Email
—
Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
695365503

Catalogue (7129)

Page 30 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment SET LWCA4525NPCRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA7035FPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA50230FNPCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60415FHAPC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4024FCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6537RS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4655FNS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50415FHBCS
FDA UDI
Class IIActive
LW Fixture LWSF8007SC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7065FHS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45215FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4577N
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6535FCRS
FDA UDI
Class IIActive
LW Oss Slot Driver HLWOSRLW
FDA UDI
Class IActive
LW Vis Abutment LWCA5045H
FDA UDI
Class IIActive
LW Angled Abutment LWAA45215FNPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7075FHC
FDA UDI
Class IIActive
LW Angled Abutment LWAA45417FHAPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7077HS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45425NS
FDA UDI
Class IIActive
LW Narrow Scan Body LWNDSB4012HS
FDA UDI
Class IActive
LW Angled Abutment LWAA50430FHAS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6077HPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7044FNS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60230FHBC
FDA UDI
Class IIActive
Point Drill HPD15C
FDA UDI
Class IActive
LW Solid Abutment LWSA6535C
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5027FPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5027HCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45417N
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4534HRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7055FHPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6065NRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6017FCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6047CRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50230FHAPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA5025FHPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4555HPC
FDA UDI
Class IIActive
LW Solid Abutment LWSA5034PC
FDA UDI
Class IIActive
LW Solid Abutment LWSA4055F
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4544FHRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6024FRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5517FPCRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA5555
FDA UDI
Class IIActive
LW Solid Abutment LWSA5527FC
FDA UDI
Class IIActive
LW Fixture LWSF4513S
FDA UDI
Class IIActive
LW Vis Abutment LWCA4665FHCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4624NS
FDA UDI
Class IIActive
LW Solid Abutment LWSA5044C
FDA UDI
Class IIActive
LW Narrow Vis Abutment SET LWNCA4527FNCRS
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Ossvis Co., Ltd. Anyang-si Gyeonggi · KR FEI 3025338240