Spex Limited
Country not established
Spex Limited is a medical device manufacturer, with 693 devices listed in FDA GUDID and EUDAMED (FDA Class I) as of 14 Nov 2026.
- Devices
- 693
Registry facts
- Registries
- FDA GUDID 693
- EUDAMED 356
- Device classes
- FDA Class I 693
- Identifiers
- DUNS 748649195
What Spex Limited makes
The company designs and manufactures wheelchair accessories, including seat cushions, back rests, prefabricated head/trunk supports, occupant restraints, and headrests for wheelchairs and standers. These products are intended to enhance comfort, support, and safety for users in seated or transitional positions.
All listed devices fall under Class I regulation and are registered in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 693 devicesShowing 1-50 of 693
Company details
- DUNS number
- 748649195
- Phone
- +64330079790
Frequently asked questions
How many devices does SPEX LIMITED have in the registry?
The registry currently lists 693 devices for SPEX LIMITED. Devices recorded under merged duplicate company entries are counted once.
Which registries list SPEX LIMITED's devices?
Among its 50 most recently registered devices, SPEX LIMITED has devices listed in EUDAMED (6 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do SPEX LIMITED's devices fall under?
Among its 50 most recently registered devices, the classes recorded for SPEX LIMITED's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from SPEX LIMITED in the registry?
The most recently registered devices listed for SPEX LIMITED include Spex Limited 1156-5822-410, Spex Limited 1255-1623-0SS-C, Spex Limited 1156-5821-410 and Spex Limited 1156-0301-120.