Imed Technology, Inc.
United StatesFDA 510(k) applicant, unverified FDA FEI 3003813437
- Devices
- 12
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
Catalogue
Search and filter all 12 devicesCompany details
- FDA FEI number
- 3003813437
- DUNS number
- 087974775
- Address
- 8720 Silverado Trail, Suite 3B, Mc Kinney, TX, 75070
FDA establishments
- I-Med Technology Maastricht Limburg · NL FEI 3033162886
Frequently asked questions
How many devices does Imed Technology, Inc. have in the registry?
The registry currently lists 12 devices for Imed Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Imed Technology, Inc.'s devices?
Among its 12 most recently registered devices, Imed Technology, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (10 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Imed Technology, Inc.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for Imed Technology, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Imed Technology, Inc. in the registry?
The most recently registered devices listed for Imed Technology, Inc. include iMed Technology Anchor Dry 5x5 iMed 5x5, iMed Technology Anchor Dry 7x7 iMed 7x7, iMed Technology Anchor Dry 12x14 iMed 12x14 and iMed Technology Anchor Dry 10x12 iMed 10x12.
Which FDA establishments are linked to Imed Technology, Inc.?
1 FDA establishment is linked to Imed Technology, Inc. in the registry; they are listed on the company page.