Is this your brand? Sign in to claim ownership.
Sign in to claim this brandVERICOM CO., LTD.
US
Last updated May 24, 2026
What VERICOM CO., LTD. makes
Vericom Co., Ltd. manufactures dental materials and devices, including ceramic-based fabrication materials for dental appliances, dental composite resins, and preformed permanent suprastructures for dental implants. Their portfolio also covers silicone impression materials for dental casts, dental etching solutions, single-use syringe needles, cavity varnishes, and bonding agents for dentine.
The company’s products are regulated as Class I and Class II medical devices under FDA guidelines and are listed in the FDA’s Unique Device Identifier (UDI) database. Vericom 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 Vericom Co., Ltd. manufacture?
Vericom Co., Ltd. specializes in dental materials and devices, including ceramic-based fabrication materials for dental appliances, dental composite resins, and preformed permanent suprastructures for dental implants. Their product range also includes silicone impression materials for dental casts, dental etching solutions, single-use syringe needles, cavity varnishes, and bonding agents for dentine. These materials are designed for use in restorative and prosthetic dental procedures.
Where is Vericom Co., Ltd. based?
Vericom Co., Ltd. is headquartered in the United States. The company’s location in the US aligns with its focus on manufacturing dental materials and devices that comply with regulatory standards applicable in North America.
Which regulatory registries list Vericom Co., Ltd.’s devices?
Vericom Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices regulated by the U.S. Food and Drug Administration, ensuring traceability and compliance with regulatory requirements.
How are Vericom Co., Ltd.’s devices classified under FDA regulations?
Vericom Co., Ltd.’s devices are classified as either Class I or Class II medical devices under FDA guidelines. Class I devices generally pose minimal risk and often require less regulatory oversight, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on the specific device type and its intended use.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- vericom.co.kr
- —
- —
- [email protected]
- Phone
- +82314412881
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 689698269
Catalogue (514)
Page 11 of 11| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Well-Paste | K090992 | FDA 510(k) | Class II | Active |
| Well-Root ST | K170950 | FDA 510(k) | Class II | Active |
| Bc Plus | K043562 | FDA 510(k) | Class II | Active |
| Eco-S | K103121 | FDA 510(k) | Class II | Active |
| Vonflex Putty | K091267 | FDA 510(k) | Class II | Active |
| Well-Pex | K080266 | FDA 510(k) | Class II | Active |
| Vonflex S Bite | K140966 | FDA 510(k) | Class II | Active |
| MAZIC Duro | K163346 | FDA 510(k) | Class II | Active |
| Denfil | K042124 | FDA 510(k) | Class II | Active |
| V-varnish Premium | K160377 | FDA 510(k) | Class II | Active |
| Denfil Flow | K060637 | FDA 510(k) | Class II | Active |
| Vonflex Heavy, Vinflex Light | K103164 | FDA 510(k) | Class II | Active |
| Denfil Etchant-37 | K080265 | FDA 510(k) | Class II | Active |
| Vonflex S Putty | K152518 | FDA 510(k) | Class II | Active |
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.
- Vericom Co., Ltd. Chuncheon-Si Gangwon · KR FEI 3003449480