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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 33 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Solid Abutment SET LWSA7044RS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4564FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7065FHC
FDA UDI
Class IIActive
Point Drill HPD23L
FDA UDI
Class IActive
LW Vis Abutment LWCA7045FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4515FHC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4534FPCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45215HA
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA7014FCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5067FHPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4647FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7035FH
FDA UDI
Class IIActive
Step Drill HSD7008C
FDA UDI
Class IActive
LW Vis Abutment LWCA6055FNC
FDA UDI
Class IIActive
LW Solid Abutment LWSA5545FC
FDA UDI
Class IIActive
LW Angled Abutment LWAA60225HBCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7055FNPCS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5037FPCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45230FHAC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4624NCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7045FHPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7034FNCS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4044PCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6055HPCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45425FHBS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45415FHAPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4554H
FDA UDI
Class IIActive
LW Vis Abutment LWCA4524HPC
FDA UDI
Class IIActive
Round Drill HRD09
FDA UDI
Class IActive
LW Vis Abutment SET LWCA7035FNRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7024FHS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5044FNCS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4047FPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5047FHPC
FDA UDI
Class IIActive
Step Drill HSD6010C
FDA UDI
Class IActive
LW Vis Abutment LWCA6044FHPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6024NPC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7025FHRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7057NPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7055HPCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45430HACS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50225FHACS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60425FHA
FDA UDI
Class IIActive
LW Vis Abutment LWCA4557FHC
FDA UDI
Class IIActive
LW Angled Abutment LWAA60225FHAC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7064FHRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4627NCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6014FNS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6055NCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45425FHAPCS
FDA UDI
Class IIActive

Related Companies

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Importers

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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