Vitrolife AB
United Statesfrom the FDA registration address FDA FEI 3002757762
Part of Vitrolife GmbH
Vitrolife AB is a medical device manufacturer, with 207 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 14 Nov 2026.
- Devices
- 207
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 203
- FDA 510(k) 4
- Device classes
- FDA Class II 197
- FDA Class I 8
- Sites and related companies
- Identifiers
- FDA FEI 3002757762
At a glance
Market reach
- United States
- FDA FEI
What Vitrolife AB makes
Vitrolife AB manufactures medical devices for assisted reproduction and laboratory use, including user-induced micropipettes such as ICSI Pipette, Biopsy Pipette, and Dissection Pipette, as well as spermatozoa/semen motility medium supplements like Enhance-S Plus and Enhance Sperm Wash, and other IVD reagents like cell culture media and specimen microscopy slides.
Catalogue
Search and filter all 207 devicesShowing 1-50 of 207
Company details
- FDA FEI number
- 3002757762
- Address
- 4940 Carroll Canyon Rd Ste 100, San Diego, CA, 92121
Frequently asked questions
How many devices does Vitrolife AB have in the registry?
The registry currently lists 207 devices for Vitrolife AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitrolife AB's devices?
Among its 50 most recently registered devices, Vitrolife AB has devices listed in FDA GUDID (50 devices).
What risk classes do Vitrolife AB's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Vitrolife AB's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitrolife AB in the registry?
The most recently registered devices listed for Vitrolife AB include ICSI Pipette 15402, ICSI Pipette 15611, Biopsy Pipette 15143 and Enhance-S Plus 15246.