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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 34 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment LWCA6077FH
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6055RS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60217FNC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7044FNC
FDA UDI
Class IIActive
LW Narrow Pre-milled Abutment LWNDPA1040HMXS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4015RS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45425FHAS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5017FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA4635FHPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7014HPC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4554NCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5075NCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4544FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4515FHS
FDA UDI
Class IIActive
LW Healing Abutment LWHA808
FDA UDI
Class IIActive
LW Narrow Cover Screw LWNCS3004C
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6544RS
FDA UDI
Class IIActive
Twist Drill HTD53C
FDA UDI
Class IActive
LW Angled Abutment LWAA50225HBPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6077NCS
FDA UDI
Class IIActive
LW Narrow Healing Abutment LWNHA409FC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7054NCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6015CRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45225FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA4647NPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6027N
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7027HRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7077FNPCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5044FHPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7045HCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45417FNPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA6034FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA4577HPC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA7017FPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4544FNRS
FDA UDI
Class IIActive
LW Fixture LWSF8008SC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4674FN
FDA UDI
Class IIActive
LW Angled Abutment LWAA50425FNCS
FDA UDI
Class IIActive
LW Fixture LWSF4007S
FDA UDI
Class IIActive
LW Vis Abutment LWCA4647HCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5025HC
FDA UDI
Class IIActive
LW Pick-up Impression Coping LWPI5011H
FDA UDI
Class IActive
Twist Drill HTD31
FDA UDI
Class IActive
LW Vis Abutment LWCA4517FNC
FDA UDI
Class IIActive
Point Drill HPD20SC
FDA UDI
Class IActive
LW Vis Abutment LWCA6064FNS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45225FHAPCS
FDA UDI
Class IIActive
Trimming Drill HTMD55
FDA UDI
Class IActive
LW Angled Abutment LWAA50417HBS
FDA UDI
Class IIActive
LW Solid Abutment LWSA4557
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

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