Invitrocare Inc
United Statesfrom the FDA registration address FDA establishment FEI 3004882774
- Devices
- 41
- Registrations
- FDA
- FDA recalls
- 0
What Invitrocare Inc makes
InvitroCare Inc manufactures sperm processing and embryo culture media for assisted reproductive technology, including sperm wash medium, IVC one, two, and three blastocyst medium, Q-HTF, HTF-HEPES, and related reagents such as hyaluronidase and PVP-polyvinylpyrrolidone.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 41 devicesCompany details
- FDA FEI number
- 3004882774
- Address
- 8415 Progress Dr Unit F, Frederick, MD, 21701
Frequently asked questions
How many devices does INVITROCARE INC have in the registry?
The registry currently lists 41 devices for INVITROCARE INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list INVITROCARE INC's devices?
Among its 41 most recently registered devices, INVITROCARE INC has devices listed in FDA 510(k) (10 devices) and FDA GUDID (31 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do INVITROCARE INC's devices fall under?
Among its 41 most recently registered devices, the classes recorded for INVITROCARE INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from INVITROCARE INC in the registry?
The most recently registered devices listed for INVITROCARE INC include SPERM FREEZING MEDIUM - SpermFreeze 2230-50, PVP - Polyvinylpyrrolidone 2210-50, HUMAN SERUM ALBUMIN (HSA) and HTF HEPES 2002-5.