O.R. Solutions, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
Catalogue
Ors-111 Ref K953654
510(k) 510(k)Dms-9000 Ref K960836
510(k) 510(k)Warmer 2000LD Ref K021289
510(k) 510(k)Ors-1000LD Ref K021288
510(k) 510(k)Ors Model 6000 Endoscope Holder Ref K051979
510(k) 510(k)1075LD Hush-Slush Ref K023283
510(k) 510(k)Ors-3000LD Ref K023282
510(k) 510(k)
Frequently asked questions
How many devices does O.R. Solutions, Inc. have in the registry?
The registry currently lists 7 devices for O.R. Solutions, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list O.R. Solutions, Inc.'s devices?
Among its 7 most recently registered devices, O.R. Solutions, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do O.R. Solutions, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for O.R. Solutions, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from O.R. Solutions, Inc. in the registry?
The most recently registered devices listed for O.R. Solutions, Inc. include ORS-111, DMS-9000, WARMER 2000LD and ORS-1000LD.