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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 31 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment SET LWCA7044FNCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4577FHCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60225HBPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7034HS
FDA UDI
Class IIActive
LW Solid Abutment LWSA5535PC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4524FNPC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7074FHPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6075FHPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6055NPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4627FHPCS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA7045FCRS
FDA UDI
Class IIActive
Step Drill HSD3513
FDA UDI
Class IActive
LW Vis Abutment LWCA6045FHC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4575HCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4614NPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6047FHCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6015HS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4654FNPC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4054PCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4644HRS
FDA UDI
Class IIActive
LW Healing Abutment LWHA707
FDA UDI
Class IIActive
LW Fixture LWSF4511SC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4534HS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4654NPCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6554RS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5064FH
FDA UDI
Class IIActive
LW Angled Abutment LWAA50425NC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7027NCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4514NCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4665FNS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4565HCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50225FHBCS
FDA UDI
Class IIActive
Twist Drill HTD55C
FDA UDI
Class IActive
LW Angled Abutment LWAA45415NPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA45230HACS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4017PCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5045HS
FDA UDI
Class IIActive
LW Solid Abutment LWSA5514C
FDA UDI
Class IIActive
LW Vis Abutment LWCA5057NCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6044HCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7055FNCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4624FHCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4667FHCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4525FHPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA50230HACS
FDA UDI
Class IIActive
LW Solid Abutment LWSA6047
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4677FNCRS
FDA UDI
Class IIActive
OSS Pick-up Impression Coping LWOPI45NS
FDA UDI
Class IActive
LW Vis Abutment LWCA4637NPCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4624NPCRS
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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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