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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 25 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment LWCA4664HPCS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6044RS
FDA UDI
Class IIActive
LW Solid Abutment LWSA7044FC
FDA UDI
Class IIActive
LW Angled Abutment LWAA50217HBCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7064NCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5017FPCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6025CRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4645FHPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4567FH
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6047FNCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6014FRS
FDA UDI
Class IIActive
LW Narrow Transfer Impression Coping LWNTI4011N
FDA UDI
Class IActive
LW Vis Abutment LWCA6054FHS
FDA UDI
Class IIActive
Straight Round Bur HSRB23
FDA UDI
Class IActive
LW Vis Abutment SET LWCA7067FHPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4655NRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5015FCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7025NRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4644FNPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7047FHPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA6025NPC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6555FPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4677FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4614FNCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4677NPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5015FH
FDA UDI
Class IIActive
LW Angled Abutment LWAA45230FNPCS
FDA UDI
Class IIActive
LW Pre-milled Abutment LWDPA1040HMX
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6014NRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6075FNCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6545PCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50415FHBPCS
FDA UDI
Class IIActive
Solid Lab Analog LWSLA707
FDA UDI
Class IActive
LW Vis Abutment LWCA7025FHPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4547FHC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4555FH
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6515PCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6044FNCS
FDA UDI
Class IIActive
LW Healing Abutment LWHA605F
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5067FNCRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA6027F
FDA UDI
Class IIActive
LW Solid Abutment LWSA6545
FDA UDI
Class IIActive
LW Narrow Vis Abutment SET LWNCA4024FNCRS
FDA UDI
Class IIActive
LL Mini Onebody Implant LLMF300835S
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5045NRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4514FNCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4674HCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5017NCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4547RS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5025FNC
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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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