Ryder Intl. Corp.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Assist(Tm) Aseptic Syringe Irrigation System Ref K881981
Regimes: 510(k) Registry: 510(k)Usci Ideal Ptca Kit Ref K953522
Regimes: 510(k) Registry: 510(k)Opti-Lens Contact Lens Case Ref K920064
Regimes: 510(k) Registry: 510(k)Kestrel Contact Lens Storage Case(Polysulfone) Ref K853727
Regimes: 510(k) Registry: 510(k)Contact Lens Case W/Postive Heat Indi. Mod. #695 Ref K870278
Regimes: 510(k) Registry: 510(k)Opti-Lens(Tm) Contact Lens Case Ref K915082
Regimes: 510(k) Registry: 510(k)Bard Eagle Inflation Device Ref K962611
Regimes: 510(k) Registry: 510(k)Ryder Lacrimal Intubationset Ref K962151
Regimes: 510(k) Registry: 510(k)Kestrel Contact Lens Storage Case(Polystyrene) Ref K853729
Regimes: 510(k) Registry: 510(k)Kestrel Contact Lens Storage Case(Noryl) Ref K853728
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ryder Intl. Corp. have in the registry?
The registry currently lists 10 devices for Ryder Intl. Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ryder Intl. Corp.'s devices?
Among its 10 most recently registered devices, Ryder Intl. Corp. has devices listed in FDA 510(k) (10 devices).
What risk classes do Ryder Intl. Corp.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Ryder Intl. Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ryder Intl. Corp. in the registry?
The most recently registered devices listed for Ryder Intl. Corp. include ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEM, USCI IDEAL PTCA KIT, OPTI-LENS CONTACT LENS CASE and KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE).