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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
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Email
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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 8 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment LWCA5035FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7034HCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60225HBPC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5545FRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA4537C
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4674FNRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA7015C
FDA UDI
Class IIActive
LW Vis Abutment LWCA7034FNPCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4525FNRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4665N
FDA UDI
Class IIActive
Round Drill HRD06
FDA UDI
Class IActive
LW Vis Abutment SET LWCA5015FNPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4655HCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4517FHRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5045FPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5014FHPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA50215FHAC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4027FPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5027FHPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA6014FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA7034N
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4524HRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4574FNPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5064HCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6045NPCS
FDA UDI
Class IIActive
Cortical Drill HCD45C
FDA UDI
Class IActive
LW Vis Abutment LWCA5077FHS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6037H
FDA UDI
Class IIActive
LW Angled Abutment LWAA60230HBPCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7055NRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5035NPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA5025HPCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6025FHPCRS
FDA UDI
Class IIActive
Short Cortical Drill HCD50SI
FDA UDI
Class IActive
LW Vis Abutment SET LWCA6055FNPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4657FHRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6557FRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA7057FPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4614NPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6055FHC
FDA UDI
Class IIActive
LW Solid Abutment LWSA6545FPC
FDA UDI
Class IIActive
LW Solid Abutment LWSA4527FPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7037FNS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6525CRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6074FH
FDA UDI
Class IIActive
LW Solid Abutment LWSA4045C
FDA UDI
Class IIActive
LW Fixture LWSF6011S
FDA UDI
Class IIActive
LW Angled Abutment LWAA45430FHB
FDA UDI
Class IIActive
LW Vis Abutment LWCA4517FHC
FDA UDI
Class IIActive
LW Solid Abutment LWSA5525PC
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