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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
—
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 37 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment LWCA6067FN
FDA UDI
Class IIActive
LW Solid Abutment LWSA5057FPC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6024HPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7077N
FDA UDI
Class IIActive
LW Angled Abutment LWAA45217HAPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4627FHC
FDA UDI
Class IIActive
LW Angled Abutment LWAA50225HB
FDA UDI
Class IIActive
LW Vis Abutment LWCA6035FHCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4577HS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60217FNCS
FDA UDI
Class IIActive
LW Solid Abutment LWSA5534C
FDA UDI
Class IIActive
LW Vis Abutment LWCA4664FNC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4647FNPCRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA6525
FDA UDI
Class IIActive
LW Narrow Vis Abutment SET LWNCA4554FHCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6075NC
FDA UDI
Class IIActive
LW Angled Abutment LWAA60415N
FDA UDI
Class IIActive
LW Narrow Transfer Impression Coping LWNTI4011HC
FDA UDI
Class IActive
LW Vis Abutment LWCA4577NC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4515FNPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4535FNPC
FDA UDI
Class IIActive
OSS Pick-up Impression Coping LWOPI45H
FDA UDI
Class IActive
LW Angled Abutment LWAA60415HBPCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45217NPCS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4025PCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45215FHBS
FDA UDI
Class IIActive
Guide Full NoMount Driver Wrench HLCNRSGF
FDA UDI
Class IActive
LW Vis Abutment LWCA7047FNPC
FDA UDI
Class IIActive
LW Solid Abutment LWSA5027C
FDA UDI
Class IIActive
LW Solid Abutment LWSA5547
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5035CRS
FDA UDI
Class IIActive
Convex Osteotome 3.5 HSOT35
FDA UDI
Class IActive
LW Solid Abutment SET LWSA6545FCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA7047FPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4535FNCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4635NRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6515FPCRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA7014
FDA UDI
Class IIActive
LW Oss Abutment Driver Engine HLWORSE
FDA UDI
Class IActive
LW Vis Abutment LWCA7015FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4537FNS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45217FNC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4635HPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5067FHCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50415HAPCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4575NCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6557PCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50425FHBPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4677NPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA60430FHBPCS
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