Oricare Inc.
United StatesFDA applicant, unverified FDA FEI 3009129579
Oricare Inc. is a medical device manufacturer, with 48 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 48
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 44
- FDA 510(k) 4
- Device classes
- FDA Class II 48
- Identifiers
- FDA FEI 3009129579
- DUNS 009527042
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 48 devicesCompany details
- FDA FEI number
- 3009129579
- DUNS number
- 009527042
- Address
- 1900 Am Dr, Quakertown, PA, 18951
- Suzy@Oricaremed.com
- Phone
- 1-215-538-2470
Frequently asked questions
How many devices does ORICARE INC. have in the registry?
The registry currently lists 48 devices for ORICARE INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ORICARE INC.'s devices?
Among its 48 most recently registered devices, ORICARE INC. has devices listed in FDA 510(k) (4 devices) and FDA GUDID (44 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ORICARE INC.'s devices fall under?
Among its 48 most recently registered devices, the classes recorded for ORICARE INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ORICARE INC. in the registry?
The most recently registered devices listed for ORICARE INC. include V8800 Critical Care Ventilator, A9800 Anesthesia Workstation, CRITICAL CARE VENTILATOR and ORICARE L2700.