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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 23 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment SET LWCA6045HRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6015FNPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4515NRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45225FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4637FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7025FH
FDA UDI
Class IIActive
LW Vis Abutment LWCA5017H
FDA UDI
Class IIActive
LW Solid Abutment LWSA7057C
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4644NRS
FDA UDI
Class IIActive
Guide Full Twist Drill HTD2211GF
FDA UDI
Class IActive
Guide Full Step Drill HSD4010GF
FDA UDI
Class IActive
LW Angled Abutment LWAA50430HBPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4515HS
FDA UDI
Class IIActive
LW Solid Abutment LWSA4054C
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7067NRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5067NPC
FDA UDI
Class IIActive
LW Fixture LWSF6507S
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4575HPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5044HRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6024FNPCS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5525RS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7015FNPCS
FDA UDI
Class IIActive
LW Solid Abutment LWSA6024PC
FDA UDI
Class IIActive
Round Drill HRD16
FDA UDI
Class IActive
LW Vis Abutment LWCA4614FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4515FNCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60417HBCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5035HPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4677FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA5057NC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4047CRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6055FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA4547NPC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6057FRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6075FNPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6014FHC
FDA UDI
Class IIActive
LW Solid Abutment LWSA4055FPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA45415FHB
FDA UDI
Class IIActive
LW Healing Abutment LWHA757F
FDA UDI
Class IIActive
Point Drill HPD13C
FDA UDI
Class IActive
LW Vis Abutment LWCA4667FNS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45217FHAS
FDA UDI
Class IIActive
Lindemann Drill HLD22C
FDA UDI
Class IActive
LW Solid Abutment LWSA5017FC
FDA UDI
Class IIActive
LW Fixture PLWSF7008SC
FDA UDI
Class IIActive
OSS Transfer Impression Coping LWOTI55HS
FDA UDI
Class IActive
LW Solid Abutment SET LWSA4555PCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60415FNPCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45417FHA
FDA UDI
Class IIActive
LW Vis Abutment LWCA6067FHCS
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