Radlink, Inc.
United StatesFDA applicant, unverified FDA FEI 3005560996
Radlink, Inc. is a medical device manufacturer, with 18 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 12 Nov 2026.
- Devices
- 18
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 16
- FDA 510(k) 2
- Device classes
- FDA Class II 15
- FDA Class I 3
- Identifiers
- FDA FEI 3005560996
- DUNS 069190036
At a glance
Market reach
- United States
- FDA FEI
What Radlink, Inc. makes
Radlink, Inc. manufactures computed radiography and digital imaging scanners, digital imaging cassettes, and X-ray film cassette holders. The company also produces electronic goniometers and kinesiology sensors, as well as radiology information systems and picture archiving and communication system digital archive devices.
These products are listed within the FDA 510(k) and FDA UDI regulatory databases.
Catalogue
Search and filter all 18 devicesCompany details
- FDA FEI number
- 3005560996
- DUNS number
- 069190036
- Address
- 2101 E El Segundo Blvd, Suite 104, El Segundo, CA, 90245
Frequently asked questions
How many devices does RADLINK, INC. have in the registry?
The registry currently lists 18 devices for RADLINK, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list RADLINK, INC.'s devices?
Among its 18 most recently registered devices, RADLINK, INC. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (16 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do RADLINK, INC.'s devices fall under?
Among its 18 most recently registered devices, the classes recorded for RADLINK, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from RADLINK, INC. in the registry?
The most recently registered devices listed for RADLINK, INC. include Radlink Cassette CAS1012, Radlink GPS Trauma, Radlink DR Tablet Retrofit DRRETRO and Radlink GPS Tablet Stand.