Peptonic Medical AB
SwedenFDA applicant, unverified FDA FEI 3019793660
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Peptonic Medical AB makes
Peptonic Medical AB manufactures VagiVital Aktivgel, a vaginal gel designed for local treatment of bacterial vaginosis, containing lactoferrin and other active components to restore vaginal flora balance.
The company’s product portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the U.S. regulatory database. The manufacturer is based in the United States.
Catalogue
VagiVital Aktivgel Ref K200098
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3019793660
- Address
- Gustavslundsvagen 143, Bromma Stockholm
Frequently asked questions
How many devices does Peptonic Medical AB have in the registry?
The registry currently lists 1 device for Peptonic Medical AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peptonic Medical AB's devices?
Among its 1 most recently registered device, Peptonic Medical AB has devices listed in FDA 510(k) (1 device).
What risk classes do Peptonic Medical AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Peptonic Medical AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Peptonic Medical AB in the registry?
The most recently registered devices listed for Peptonic Medical AB include VagiVital Aktivgel.