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Sign in to claim this brandCARGUS INTERNATIONAL, INC
US
Last updated May 24, 2026
What CARGUS INTERNATIONAL, INC makes
Cargus International, Inc. manufactures reusable diamond dental burs, single-use dental impression trays, and silicone dental impression materials for dental procedures. Their portfolio also includes nitrile examination gloves, dental bibs, sterilization container liners, surgical/medical face masks, and dentifrice for oral hygiene.
The company’s products are classified under FDA’s Class I and Class II regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 does Cargus International, Inc. manufacture?
Cargus International, Inc. produces dental products including reusable diamond dental burs, single-use dental impression trays, silicone dental impression materials, nitrile examination gloves, dental bibs, sterilization container liners, surgical/medical face masks, and dentifrice for oral hygiene.
Where is Cargus International, Inc. based?
Cargus International, Inc. operates from the United States, as indicated in their device registration information.
Which regulatory registries list Cargus International, Inc.'s devices?
The company's devices are listed in the FDA's Unique Device Identifier (UDI) database, which tracks medical devices marketed in the United States.
How are Cargus International, Inc.'s devices classified?
The company's products are classified under FDA regulations as Class I and Class II medical devices, with Class I being lower risk and Class II requiring more regulatory controls.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- cargus.com
- —
- —
- [email protected]
- Phone
- 845-267-2600
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 096191093
Catalogue (480)
Page 10 of 10| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mark3 | 6119 | FDA UDI | Class II | Active |
| Mark3 | 862-014XF | FDA UDI | Class I | Active |
| Mark3 | 805-016C | FDA UDI | Class I | Active |
| Mark3 | 1973BL | FDA UDI | Class II | Active |
| Mark3 | 6115 | FDA UDI | Class II | Active |
| Mark3 | 4884 | FDA UDI | Class II | Active |
| Mark3 | 379-023M | FDA UDI | Class I | Active |
| Mark3 | 6129 | FDA UDI | Class II | Active |
| Mark3 | 3013BULK | FDA UDI | Class II | Active |
| Mark3 | 1952 | FDA UDI | Class I | Active |
| Mark3 | 859-016F | FDA UDI | Class I | Active |
| Mark3 | 886-016C | FDA UDI | Class I | Active |
| Mark3 | 4885 | FDA UDI | Class II | Active |
| Mark3 | 1971WH | FDA UDI | Class II | Active |
| Mark3 | 878-012C | FDA UDI | Class I | Active |
| Mark3 | 3004 | FDA UDI | Class II | Active |
| Mark3 | 1145BULK | FDA UDI | Class II | Active |
| Mark3 | 9092 | FDA UDI | Class II | Active |
| Mark3 | 4886 | FDA UDI | Class II | Active |
| Mark3 | 846KR-016M | FDA UDI | Class I | Active |
| Mark3 | 1950CS | FDA UDI | Class I | Active |
| Mark3 | 1971LA | FDA UDI | Class II | Active |
| Mark3 | 9091 | FDA UDI | Class II | Active |
| Mark3 | 855-017F | FDA UDI | Class I | Active |
| Mark3 | 0221 | FDA UDI | Class II | Active |
| Mark3 | 2226 | FDA UDI | Class I | Active |
| Mark3 | 1951 | FDA UDI | Class I | Active |
| Mark3 | 856-016C | FDA UDI | Class I | Active |
| Mark3 | 6111 | FDA UDI | Class II | Active |
| Mark3 | 848-018XC | FDA UDI | Class I | Active |
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