Produits Dentaires Pierre Rolland (Acteon Group) is one of 293 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Produits Dentaires Pierre Rolland (Acteon Group) - FDA 510(k) Cleared...
Recent clearances: EXPAZEN
1
Total
1
Cleared
0
Denied
Produits Dentaires Pierre Rolland (Acteon Group) has 1 FDA 510(k) cleared medical devices. Based in Merignac, FR.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Produits Dentaires Pierre Rolland (Acteon Group) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acteon, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Produits Dentaires Pierre Rolland (Acteon Group)
1 devices