Coaptech, Inc.
United StatesFDA applicant, unverified FDA FEI 3015177732
- Devices
- 17
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 17 devicesCompany details
- FDA FEI number
- 3015177732
- DUNS number
- 080322442
- Address
- 101 W. Dickman Street, Suite 700, Baltimore, MD, 21230
- [email protected]
- Phone
- 1 443 574 6934
Frequently asked questions
How many devices does Coaptech, Inc. have in the registry?
The registry currently lists 17 devices for Coaptech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coaptech, Inc.'s devices?
Among its 17 most recently registered devices, Coaptech, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (14 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Coaptech, Inc.'s devices fall under?
Among its 17 most recently registered devices, the classes recorded for Coaptech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Coaptech, Inc. in the registry?
The most recently registered devices listed for Coaptech, Inc. include PUMA-G Pediatric System™ 0010400, PUMA-G Pediatric System™ 0010380, PUMA-G System™ 0010204 and PUMA-G System™ 0010323.