Dyna Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
What Dyna Corp. makes
Dyna Corp. manufactures patient transport and emergency medical equipment, including roll-in ambulance cots and folding stretchers. Their products include the DYNA GLIDE 2600 roll-in ambulance cot and the HARE emergency stretcher variants, designed for pre-hospital and emergency care settings. The portfolio also covers loading aids like the HARE Model 2000 EZ Loader.
The company’s devices are regulated under FDA’s 510(k) pathway, with products classified as Class I and Class II. These items are listed in the FDA’s 510(k) database, reflecting their authorised status in the US market. The manufacturer operates from the United States.
Catalogue
Dyna Glide 2600 Roll-In Ambulance Cot (95759) Ref K972528
510(k) 510(k)Hare Emergency Stretcher Ref K900670
510(k) 510(k)Hare Emergency Stretcher With Wheels Ref K900671
510(k) 510(k)Hare Folding Back Emergency Stretcher Ref K902503
510(k) 510(k)Hare Model 2000 Ez Loader Model 95555 Ref K962181
510(k) 510(k)
Frequently asked questions
How many devices does Dyna Corp. have in the registry?
The registry currently lists 5 devices for Dyna Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dyna Corp.'s devices?
Among its 5 most recently registered devices, Dyna Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Dyna Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Dyna Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dyna Corp. in the registry?
The most recently registered devices listed for Dyna Corp. include DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759), HARE EMERGENCY STRETCHER, HARE EMERGENCY STRETCHER WITH WHEELS and HARE FOLDING BACK EMERGENCY STRETCHER.