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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
—
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 27 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Solid Abutment SET LWSA5024CRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4545HPC
FDA UDI
Class IIActive
Saw Disc HSSD80
FDA UDI
Class IActive
Guide Full Step Drill HSD4507GF
FDA UDI
Class IActive
LW Vis Abutment SET LWCA4657HCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4635FNS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45425FNPC
FDA UDI
Class IIActive
Twist Drill HTD46C
FDA UDI
Class IActive
LW Vis Abutment LWCA5014NPCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5037NRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45415NCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5015NPCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7065NRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6027HPC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4655FNPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5025FNS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50225FHA
FDA UDI
Class IIActive
Point Drill HPD15S
FDA UDI
Class IActive
LW Fixture LWSF6007S
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5024FNRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5555PCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4045FPCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60417FNC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6555CRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5035FH
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6537PCRS
FDA UDI
Class IIActive
LW Narrow Healing Abutment LWNHA458FC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4627HCS
FDA UDI
Class IIActive
LW Solid Abutment LWSA6544FC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5037CRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA7044PCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5075HCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4547PCRS
FDA UDI
Class IIActive
LW Fixture LWSF7513SC
FDA UDI
Class IIActive
Twist Drill HTD54
FDA UDI
Class IActive
LW Vis Abutment LWCA6035FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA7017FH
FDA UDI
Class IIActive
LW Solid Abutment LWSA6557F
FDA UDI
Class IIActive
LW Angled Abutment LWAA45217FNS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4647NPCRS
FDA UDI
Class IIActive
Step Drill HSD3513C
FDA UDI
Class IActive
LW Angled Abutment LWAA50430FHBC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5045FNRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4634HPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4654HPCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60215HACS
FDA UDI
Class IIActive
LW Solid Abutment LWSA4055PC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4525NCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50225FN
FDA UDI
Class IIActive
LW Healing Abutment LWHA409F
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