Surmodics, Inc.
United StatesFDA applicant, unverified FDA FEI 3014687026
Surmodics, Inc. is a medical device manufacturer, with 64 devices listed in FDA GUDID, FDA 510(k) and FDA PMA (FDA Class II and III) as of 15 Nov 2026.
- Devices
- 64
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 52
- FDA 510(k) 11
- FDA PMA 1
- Device classes
- FDA Class II 41
- FDA Class III 23
- Identifiers
- FDA FEI 3014687026
- DUNS 098414659
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 64 devicesShowing 1-50 of 64
Company details
- FDA FEI number
- 3014687026
- DUNS number
- 098414659
- Address
- 7905 Golden Triangle Drive Suite 190, Eden Prairie, MN, 55344
Frequently asked questions
How many devices does Surmodics, Inc. have in the registry?
The registry currently lists 64 devices for Surmodics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surmodics, Inc.'s devices?
Among its 50 most recently registered devices, Surmodics, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Surmodics, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Surmodics, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Surmodics, Inc. in the registry?
The most recently registered devices listed for Surmodics, Inc. include Pounce Sheath PFS-0035-16F14, Sublime Microcatheter, 018, 200cm, Angle SRA-MC18-ANG200, Sublime Microcatheter, 014, 150cm, Angle SRA-MC14-ANG150 and Pounce ™ XL Thrombectomy PTS-1011-7F135.