Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
695365503

Catalogue (7129)

Page 22 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Vis Abutment LWCA4667FHC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7045HCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA50225HAS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4654NC
FDA UDI
Class IIActive
LW Vis Abutment LWCA7074FNC
FDA UDI
Class IIActive
LW Vis Abutment LWCA5054FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4544FHPC
FDA UDI
Class IIActive
LW Angled Abutment LWAA60217FHACS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5077FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA4545FNPC
FDA UDI
Class IIActive
LW Solid Abutment LWSA5044PC
FDA UDI
Class IIActive
LW Solid Abutment LWSA6054F
FDA UDI
Class IIActive
LW Solid Abutment LWSA5015C
FDA UDI
Class IIActive
Parallel Pin HPP3523
FDA UDI
Class IActive
LW Vis Abutment SET LWCA4535HCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5015FHC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5067NRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4614FNPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4627FHCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6015HPCRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60225NS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4624H
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA5514FRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4025RS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5027FN
FDA UDI
Class IIActive
LW Vis Abutment LWCA6045FNCS
FDA UDI
Class IIActive
Cortical Drill HCD35C
FDA UDI
Class IActive
LW Healing Abutment LWHA556F
FDA UDI
Class IIActive
LW Fixture LWSF4510S
FDA UDI
Class IIActive
LW Angled Abutment LWAA45430HA
FDA UDI
Class IIActive
LW Vis Abutment LWCA6055NPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4675HCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5055HPCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60230NCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5064HC
FDA UDI
Class IIActive
LW Vis Abutment LWCA6045NPC
FDA UDI
Class IIActive
LW Narrow Vis Abutment SET LWNCA4057FHCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6045HC
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6527FPCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7077FNCS
FDA UDI
Class IIActive
LW Angled Abutment LWAA60225HA
FDA UDI
Class IIActive
Short Twist Drill HTD22SI
FDA UDI
Class IActive
LW Vis Abutment SET LWCA4634FNRS
FDA UDI
Class IIActive
LW Solid Abutment LWSA5014C
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4524CRS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45230FNS
FDA UDI
Class IIActive
LW Solid Abutment LWSA6047C
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6015FRS
FDA UDI
Class IIActive
Surgical Master Kit2 SMK2
FDA UDI
Class IActive
LW Vis Abutment LWCA6044FHCS
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Ossvis Co., Ltd. Anyang-si Gyeonggi · KR FEI 3025338240