Multicept, Aps.
DenmarkFDA applicant, unverified
- Devices
- 2
What Multicept, Aps. makes
Multicept, Aps. manufactures medical devices designed for fertility and reproductive health, including the VIBRECTOR and the FERTICARE Personal Therapeutic Vibrator. These products are intended for use in assisted reproductive procedures and fertility treatments, providing vibrational stimulation for specific medical applications.
The company’s portfolio includes devices classified as Class II and Class U under regulatory frameworks, with products listed via the FDA’s 510(k) pathway. These devices are registered in the United States, where the manufacturer is based.
Catalogue
Vibrector Ref K851646
Regimes: 510(k) Registry: 510(k)Ferticare Personal Therapeutic Vibrator Ref K955589
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Multicept, Aps. have in the registry?
The registry currently lists 2 devices for Multicept, Aps.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Multicept, Aps.'s devices?
Among its 2 most recently registered devices, Multicept, Aps. has devices listed in FDA 510(k) (2 devices).
What risk classes do Multicept, Aps.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Multicept, Aps.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Multicept, Aps. in the registry?
The most recently registered devices listed for Multicept, Aps. include VIBRECTOR and FERTICARE PERSONAL THERAPEUTIC VIBRATOR.