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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
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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 26 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment LWCA6047HPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4655FHPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA45415FNC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4547N
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4545CRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50425FNS
FDA UDI
Class IIActive
LW Fixture LWSF6013S
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4537HCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5034HS
FDA UDI
Class IIActive
LW Solid Abutment LWSA7017FC
FDA UDI
Class IIActive
LW Vis Abutment LWCA6014NCS
FDA UDI
Class IIActive
LW Solid Abutment LWSA6554F
FDA UDI
Class IIActive
LW Angled Abutment LWAA60217HA
FDA UDI
Class IIActive
LW Solid Abutment LWSA6527FC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4525NPCS
FDA UDI
Class IIActive
LW Fixture PLWSF6007SC
FDA UDI
Class IIActive
LW Vis Abutment LWCA5074NC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7024HC
FDA UDI
Class IIActive
LW Solid Abutment LWSA5035PC
FDA UDI
Class IIActive
LW Angled Abutment LWAA60425HBPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5035NC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4614FHPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7014H
FDA UDI
Class IIActive
LW Angled Abutment LWAA45217NPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA6035HPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5075FHCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7027N
FDA UDI
Class IIActive
LW Fixture PLWSF4515SC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5037NCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6037FHPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7057HC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5045HPCRS
FDA UDI
Class IIActive
LW Fixture PLWSF7507SC
FDA UDI
Class IIActive
Guide Full NoMount Driver Engine HNNRLEGF
FDA UDI
Class IActive
LW Vis Abutment LWCA6077HC
FDA UDI
Class IIActive
LW Solid Abutment LWSA4025F
FDA UDI
Class IIActive
LW Angled Abutment LWAA50217FHAPCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45230FNPC
FDA UDI
Class IIActive
Step Drill HSD6015C
FDA UDI
Class IActive
LW Solid Abutment LWSA4037
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4564FHPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6044FHCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4524FNRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5554FPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7024N
FDA UDI
Class IIActive
LW Transfer Impression Coping LWTI5016NS
FDA UDI
Class IActive
LL Mini Onebody Implant LLMF251040S
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4645FHRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5027NCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6044FPCRS
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