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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
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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 35 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Solid Abutment LWSA5524PC
FDA UDI
Class IIActive
LW Angled Abutment LWAA50430FN
FDA UDI
Class IIActive
Twist Drill HTD27
FDA UDI
Class IActive
LW Vis Abutment LWCA4577NCS
FDA UDI
Class IIActive
LW Abutment Screw LWAW83
FDA UDI
Class IIActive
LW Vis Abutment LWCA4567NC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4567N
FDA UDI
Class IIActive
LW Solid Abutment LWSA4054FPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA6077H
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA7057CRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60430FHAPC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6025FHRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50225FHAPCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50415FHBC
FDA UDI
Class IIActive
LW Solid Abutment LWSA6055FC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6044NRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45217FHACS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6045FNC
FDA UDI
Class IIActive
LW Solid Abutment LWSA7017FPC
FDA UDI
Class IIActive
Point Drill HPD22SC
FDA UDI
Class IActive
LW Solid Abutment LWSA5527F
FDA UDI
Class IIActive
LW Healing Abutment LWHA467F
FDA UDI
Class IIActive
LW Healing Abutment LWHA705
FDA UDI
Class IIActive
LW Vis Abutment LWCA7077FHCS
FDA UDI
Class IIActive
Twist Drill HTD37C
FDA UDI
Class IActive
LW Healing Abutment LWHA759F
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6024PCRS
FDA UDI
Class IIActive
Trimming Drill HTMD90
FDA UDI
Class IActive
LW Solid Abutment LWSA4554
FDA UDI
Class IIActive
LW Vis Abutment LWCA5035NS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4524NPCRS
FDA UDI
Class IIActive
Round Drill HRD28
FDA UDI
Class IActive
LW Vis Abutment LWCA6057N
FDA UDI
Class IIActive
LW Vis Abutment LWCA7057N
FDA UDI
Class IIActive
LW Vis Abutment LWCA7055FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4645FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5027FHS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7034FH
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4665HCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7035FHPCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6037FHCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5075HC
FDA UDI
Class IIActive
LW Vis Abutment LWCA5064FHPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5047FNCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45225NC
FDA UDI
Class IIActive
LW Angled Abutment LWAA45225FNPC
FDA UDI
Class IIActive
LW UCLA Abutment LWUA453FNS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4525CRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5015FNRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4674FHS
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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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