D. E. Hokanson, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000007949 FEI 3019130
D. E. Hokanson, Inc. is a medical device manufacturer based in the United States, with 258 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I; EU Class I) as of 13 Nov 2026.
- Devices
- 258
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 232
- EUDAMED 43
- FDA 510(k) 19
- Device classes
- FDA Class II 219
- EU Class I 38
- FDA Class I 1
- Top EMDN categories
- Sites and related companies
- MedEnvoy Global BV authorised representative
- Identifiers
- EUDAMED SRN US-MF-000007949
- FDA FEI 3019130
- DUNS 071829634
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
- Authorised rep.
- MedEnvoy Global BVNL
What D. E. Hokanson, Inc. makes
The company manufactures reusable and single-use blood pressure cuffs, limb plethysmographs for vascular testing, and peripheral vascular haemodynamic measurement software. It also produces noninvasive vascular ultrasound systems, including probes, along with plethysmography phototransducers and paper chart recorders for diagnostic use.
These devices are classified as Class I or Class II under regulatory frameworks, with listings in the EUDAMED database, FDA’s 510(k) premarket notifications, and FDA’s Unique Device Identifier (UDI) registry. The company is based in the United States.
Catalogue
Search and filter all 258 devicesShowing 1-50 of 258
Company details
- EUDAMED SRN
- US-MF-000007949
- FDA FEI number
- 3019130
- DUNS number
- 071829634
- EUDAMED status
- Active
- EUDAMED registered name
- D. E. Hokanson, Inc.
- EUDAMED abbreviated name
- Hokanson
- Registered address
- 12840, NE 21st Place, 98005, Bellevue, United States
- Website
- www.hokansonvascular.com
- Phone
- (USA) 425-882-1689
- PRRC contact
- Robert Melloy
From the company website
Hokanson Vascular is the leading manufacturer for vascular cuffs and diagnostic peripheral vascular screening devices.
Frequently asked questions
How many devices does D. E. Hokanson, Inc. have in the registry?
The registry currently lists 258 devices for D. E. Hokanson, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D. E. Hokanson, Inc.'s devices?
Among its 50 most recently registered devices, D. E. Hokanson, Inc. has devices listed in EUDAMED (1 device) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do D. E. Hokanson, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for D. E. Hokanson, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D. E. Hokanson, Inc. in the registry?
The most recently registered devices listed for D. E. Hokanson, Inc. include Hokanson 03845, Hokanson 03844, Hokanson 03843 and Hokanson 03842.