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Sign in to claim this brandOssvis 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
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- Website
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- Phone
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- 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 28 of 143| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| LW Vis Abutment SET | LWCA5025NCRS | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA4634FHPCS | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA7017FN | FDA UDI | Class II | Active |
| 1.2 HEX Driver Engine | HHR12XE | FDA UDI | Class I | Active |
| LW Vis Abutment | LWCA4665HPC | FDA UDI | Class II | Active |
| Cortical Drill | HCD70 | FDA UDI | Class I | Active |
| LW Vis Abutment SET | LWCA7027HPCRS | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA5027NPCS | FDA UDI | Class II | Active |
| LW Angled Abutment | LWAA50415FHBS | FDA UDI | Class II | Active |
| LW Vis Abutment SET | LWCA7017NRS | FDA UDI | Class II | Active |
| LW Vis Abutment SET | LWCA7074HRS | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA4627FNPC | FDA UDI | Class II | Active |
| LW Angled Abutment | LWAA60225FNC | FDA UDI | Class II | Active |
| LW Vis Abutment SET | LWCA4657HRS | FDA UDI | Class II | Active |
| LW Angled Abutment | LWAA45225FHA | FDA UDI | Class II | Active |
| LW Fixture | LWSF5013S | FDA UDI | Class II | Active |
| LW Oss Abutment Scan Body | LWOSB558HS | FDA UDI | Class I | Active |
| LW Vis Abutment SET | LWCA4544FHCRS | FDA UDI | Class II | Active |
| LW Solid Abutment | LWSA4055C | FDA UDI | Class II | Active |
| LW Solid Abutment | LWSA5545F | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA4675FHC | FDA UDI | Class II | Active |
| LW Solid Abutment | LWSA6024C | FDA UDI | Class II | Active |
| LW Vis Abutment SET | LWCA4534NPCRS | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA7054FHC | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA4574HPCS | FDA UDI | Class II | Active |
| LW Fixture | LWSF8011SC | FDA UDI | Class II | Active |
| Round Drill | HRD18 | FDA UDI | Class I | Active |
| LW Vis Abutment SET | LWCA4654NRS | FDA UDI | Class II | Active |
| Guide Drill | HGMGD1310 | FDA UDI | Class I | Active |
| LW Vis Abutment | LWCA4625FHPC | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA4544HC | FDA UDI | Class II | Active |
| LW Vis Abutment SET | LWCA4517FHPCRS | FDA UDI | Class II | Active |
| LW Fixture | LWSF5511SC | FDA UDI | Class II | Active |
| LW Vis Abutment SET | LWCA6015FNCRS | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA4637FNPCS | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA5075FNS | FDA UDI | Class II | Active |
| Step Drill | HSD4510 | FDA UDI | Class I | Active |
| LL Mini Onebody Implant | LLMF301135S | FDA UDI | Class II | Active |
| LW Vis Abutment SET | LWCA4554FNPCRS | FDA UDI | Class II | Active |
| LW Vis Abutment SET | LWCA4627HRS | FDA UDI | Class II | Active |
| LW Angled Abutment | LWAA50430HAPCS | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA5044NPC | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA7077NPCS | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA5024NC | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA7045NC | FDA UDI | Class II | Active |
| LW Solid Abutment | LWSA7034F | FDA UDI | Class II | Active |
| LW Healing Abutment | LWHA408 | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA6067HPC | FDA UDI | Class II | Active |
| LW Vis Abutment | LWCA4524FHPC | FDA UDI | Class II | Active |
| LW Solid Abutment | LWSA5525 | FDA UDI | Class II | Active |
Related Companies
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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