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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
—
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 29 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment SET LWCA4617FHCRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA6524PC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6057HRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4534FNPC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5054HRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4514FNPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5064FNCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4655FNC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7034NCS
FDA UDI
Class IIActive
LW Solid Abutment LWSA6027FPC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6044CRS
FDA UDI
Class IIActive
LW Retraction Cap LWRC405
FDA UDI
Class IIActive
LW Vis Abutment LWCA5064FNPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4625FNC
FDA UDI
Class IIActive
LW Angled Abutment LWAA45225FNPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4677NS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4574NCS
FDA UDI
Class IIActive
LW Transfer Impression Coping LWTI7011H
FDA UDI
Class IActive
LW Vis Abutment SET LWCA4517NPCRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA4554FC
FDA UDI
Class IIActive
LW Solid Abutment LWSA6035FPC
FDA UDI
Class IIActive
Step Drill HSD5007
FDA UDI
Class IActive
LW Healing Abutment LWHA604
FDA UDI
Class IIActive
LW Solid Abutment LWSA6535PC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5054FCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4555FNCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6045FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4544FN
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4574NCRS
FDA UDI
Class IIActive
Harvesting Drill HHD5007
FDA UDI
Class IActive
LW Vis Abutment LWCA4625FH
FDA UDI
Class IIActive
LW Solid Abutment LWSA4045F
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4047PCRS
FDA UDI
Class IIActive
LW Healing Abutment LWHA503F
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4544HRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4675FHPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5057FNS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7035NCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50230FHBCS
FDA UDI
Class IIActive
Step Drill HSD3508
FDA UDI
Class IActive
LW Vis Abutment LWCA7027FHC
FDA UDI
Class IIActive
LW Vis Abutment LWCA5075HPC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7037HRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6035FNRS
FDA UDI
Class IIActive
LW Narrow Vis Abutment SET LWNCA4554FNCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7044FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA4635NPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA60230FNPCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60217FHBC
FDA UDI
Class IIActive
Step Drill HSD4008C
FDA UDI
Class IActive

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