Colorado Therapeutics, LLC
United StatesFDA applicant, unverified FDA FEI 3012547639
- Devices
- 14
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Colorado Therapeutics, LLC makes
Colorado Therapeutics, LLC manufactures abdominal hernia surgical mesh made from collagen with antimicrobial properties. The specific product is the Colorado Therapeutics Xenograft Implant.
The device is classified as Class II and is listed in the FDA 510(k) and FDA UDI registries. The company is based in the United States.
Catalogue
Search and filter all 14 devicesCompany details
- FDA FEI number
- 3012547639
- DUNS number
- 080356428
- Address
- 486 South Pierce Avenue Suite A, Louisville, CO, 80027
- [email protected]
- Phone
- 3034699459
Frequently asked questions
How many devices does Colorado Therapeutics, LLC have in the registry?
The registry currently lists 14 devices for Colorado Therapeutics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Colorado Therapeutics, LLC's devices?
Among its 14 most recently registered devices, Colorado Therapeutics, LLC has devices listed in FDA 510(k) (2 devices) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Colorado Therapeutics, LLC's devices fall under?
Among its 14 most recently registered devices, the classes recorded for Colorado Therapeutics, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Colorado Therapeutics, LLC in the registry?
The most recently registered devices listed for Colorado Therapeutics, LLC include Colorado Therapeutics Xenograft Implant XI-S+ and Colorado Therapeutics Xenograft Implant.