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 36 of 143
DeviceModel / ReferenceRegistriesClassStatus
LW Solid Abutment LWSA7014FPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA5024FHPCS
FDA UDI
Class IIActive
LC Pick-up Impression Coping LCPI4805OS
FDA UDI
Class IActive
LW Vis Abutment LWCA4657HC
FDA UDI
Class IIActive
LW Solid Abutment LWSA5024
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA5014FNCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA5014NPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4627HC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4654NCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4514FPCRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4525FHRS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4545HRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4677FHPCS
FDA UDI
Class IIActive
Harvesting Drill HHD3507C
FDA UDI
Class IActive
LW Fixture LWSF8013SC
FDA UDI
Class IIActive
Step Drill HSD5011C
FDA UDI
Class IActive
LW Transfer Impression Coping LWTI4511HS
FDA UDI
Class IActive
LW Vis Abutment LWCA6017N
FDA UDI
Class IIActive
LW Healing Abutment LWHA504F
FDA UDI
Class IIActive
LW Fixture PLWSF7513SC
FDA UDI
Class IIActive
Step Drill HSD5307C
FDA UDI
Class IActive
LW Vis Abutment LWCA5015N
FDA UDI
Class IIActive
Step Drill HSD5511C
FDA UDI
Class IActive
Point Drill HPD15LC
FDA UDI
Class IActive
LW Vis Abutment LWCA6074HS
FDA UDI
Class IIActive
LW UCLA Abutment LWUA451FNS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7074FNPC
FDA UDI
Class IIActive
Round Drill HRD21
FDA UDI
Class IActive
LW Vis Abutment SET LWCA7025FNRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4644HC
FDA UDI
Class IIActive
LL Mini Onebody Implant LLMF251140S
FDA UDI
Class IIActive
LW Vis Abutment LWCA7024HCS
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4677FNRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA6044HC
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA6067HRS
FDA UDI
Class IIActive
Cortical Drill HCD40
FDA UDI
Class IActive
LW Vis Abutment LWCA7027H
FDA UDI
Class IIActive
LW Solid Abutment LWSA6054C
FDA UDI
Class IIActive
LW Solid Abutment LWSA6055C
FDA UDI
Class IIActive
LW Vis Abutment SET LWCA4517NCRS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA4544FCRS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4617FNPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4557HCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4675HPC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4625HS
FDA UDI
Class IIActive
LW Angled Abutment LWAA45425HBCS
FDA UDI
Class IIActive
LW Solid Abutment SET LWSA6525RS
FDA UDI
Class IIActive
LW Vis Abutment LWCA7064NPCS
FDA UDI
Class IIActive
LW Vis Abutment LWCA4677FNC
FDA UDI
Class IIActive
LW Vis Abutment LWCA4614FHPCS
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