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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 38 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Transfer Impression Coping LWTI6011H
FDA UDI
Class IActive
LW Solid Abutment LWSA4534C
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6035HRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7045NS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6017PCRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA5524F
FDA UDI
Class IIActive
Round Drill HRD33
FDA UDI
Class IActive
LW Solid Abutment LWSA6524F
FDA UDI
Class IIActive
LW Solid Abutment LWSA7045
FDA UDI
Class IIActive
LW Healing Abutment LWHA453
FDA UDI
Class IIActive
LC Pick-up Impression Coping LCPI6005O
FDA UDI
Class IActive
LW Vis Abutment SET LWCA6014FHPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4554HRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5057FPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5067NPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5015HCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA7035PCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4655FH
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA7027NRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6035FNCRS
FDA UDI
Class IIActive
LW Fixture PLWSF5015SC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4527FHCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7077HC
FDA UDI
Class IIActive
LW Vis Abutment LWCA6067FHPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4654FNCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6055FHPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA45217FHAC
FDA UDI
Class IIActive
Sinus Drill Stopper HSDS04
FDA UDI
Class IActive
LW Angled Abutment LWAA60215HAC
FDA UDI
Class IIActive
LW Solid Abutment LWSA5554C
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4554HCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4555FNC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4645FNCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5047NPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA50225FHAC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4615FNCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4575HRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4574FHCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4555HPCS
FDA UDI
Class IIActive
LW Fixture PLWSF8011SC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4674FNCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4637NC
FDA UDI
Class IIActive
LW Vis Abutment LWCA5024HC
FDA UDI
Class IIActive
LW Angled Abutment LWAA60425FHBCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4625HCRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA5035C
FDA UDI
Class IIActive
LW Vis Abutment LWCA5065FNCS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4025FPCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60417HAPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA6024NS
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