Fertipro NV
Country not established
Part of FertiPro
Fertipro NV is a medical device manufacturer, with 47 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 15 Nov 2026.
- Devices
- 47
Registry facts
- Registries
- FDA GUDID 44
- FDA 510(k) 3
- Device classes
- FDA Class II 44
- FDA Class I 3
- Sites and related companies
- Identifiers
- DUNS 373904101
What Fertipro NV makes
Fertipro NV manufactures cryopreservation media and devices for assisted reproductive technology, including solutions for freezing and thawing sperm and embryos. Their products include VitriFreeze and VitriThaw for vitrification processes, as well as SpermFreeze and SpermFreeze SSP for sperm cryopreservation.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI registries. The company operates from the United States.
Catalogue
Search and filter all 47 devicesCompany details
- DUNS number
- 373904101
- info@fertipro.com
- Phone
- +3250791805
Frequently asked questions
How many devices does Fertipro NV have in the registry?
The registry currently lists 47 devices for Fertipro NV. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fertipro NV's devices?
Among its 47 most recently registered devices, Fertipro NV has devices listed in FDA 510(k) (3 devices) and FDA GUDID (44 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Fertipro NV's devices fall under?
Among its 47 most recently registered devices, the classes recorded for Fertipro NV's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fertipro NV in the registry?
The most recently registered devices listed for Fertipro NV include VitriFreeze VF1001, Sil-Select Plus Upper Layer SIP025UP (2,5ml), VitriFreeze VPI005 and LeucoScreen Reagent 1 LEUCO_1.