Septodont
United Statesfrom the FDA registration address FDA FEI 3008242564
Septodont is a medical device manufacturer, with 154 devices listed in FDA GUDID, FDA 510(k) and EUDAMED (FDA Class II, Unclassified and Class I) as of 12 Nov 2026.
- Devices
- 154
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 133
- FDA 510(k) 21
- EUDAMED 1
- Device classes
- FDA Class II 145
- FDA Unclassified 4
- FDA Class I 3
- Identifiers
- FDA FEI 3008242564
At a glance
Market reach
- United States
- FDA establishment
Catalogue
Search and filter all 154 devicesShowing 1-50 of 154
Company details
- FDA FEI number
- 3008242564
- Address
- 205 Granite Run Dr., Suite 150, Lancaster, PA, 17601
FDA establishments
- Septodont CEDEX Val-de-Marne · FR FEI 1000477999
Frequently asked questions
How many devices does Septodont have in the registry?
The registry currently lists 154 devices for Septodont. Devices recorded under merged duplicate company entries are counted once.
Which registries list Septodont's devices?
Among its 50 most recently registered devices, Septodont has devices listed in FDA GUDID (50 devices).
What risk classes do Septodont's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Septodont's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Septodont in the registry?
The most recently registered devices listed for Septodont include Synapse Dental Pain Eraser-Professional Use 01M0001, Synapse Dental Pain Eraser-Home Use 01M0002, Novocol GRANITEC PRIMER 9ML FP-NOVOINC-140 and SEPTODONT IMAGE MH LC REF SYR C3- 4.5G 01C2092.
Which FDA establishments are linked to Septodont?
1 FDA establishment is linked to Septodont in the registry; they are listed on the company page.