DEEP Company
FR-MF-000009485 · France · JANNEYRIAS
DEEP Company is registered in the European database on medical devices as a manufacturer, with 84 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 79 |
|---|---|
| Class IIb | 5 |
Most frequent device types declared: ANC-PROL, DESIGN, DESIGN I, LIKE A.
Among these devices, 3 are declared sterile, 5 implantable, 79 reusable.
Devices declared under this manufacturer
- Design I implant 3,5 diameter - 10 mm lenght
- Healing Abutment 4 diameter - 1 mm height
- Long final drill - 5 mm diameter
- Long final drill without stop - 4 mm diameter
- Long stepped drill - 2,7 / 3,7 diameter
- Long stepped drill without stop - 3,2 / 4,2 diameter
- Long stepped drill without stop - 3,7 / 4,7 diameter
- Short final drill - 5 mm diameter
- Ø2 mm drill stop - Long 8
- Ø2,3/Ø3,2mm, Ø3,5 mm diameter drill stop - Long 6
- Ø2,3/Ø3,2mm, Ø3,5mm diameter drill stop - short 8 / long 12
- Ø2,7/Ø3,7, Ø4 drill stop - short 6 / long 10
Showing 12 of 84 declared devices.
Catalogue references include ANC-PROL, PFD30-I91004000, PFD30-I91005060, PFD30-I91015000, PFD30-I91035000, PFD30-I92033506.
European nomenclature codes declared: L1508, L159099, P01020101, P01020180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 84 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 84 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. DEEP Company was not found in either the U.S. or the Canadian register.