MADESPA, S.A.
ES-MF-000003915 · Spain · Toledo
MADESPA, S.A. is registered in the European database on medical devices as a manufacturer, with 29 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 29 |
|---|
Devices declared under this manufacturer
- AKRYON
- ID LIGHT BODY REGULAR 4x50 ml
- ID PREMIUM REGISTRO DE MORDIDA 2x50 ml+12 MIXING TIPS
- ID PREMIUM SILICONA FAST PUTTY SOFT 250+250 ml
- ID PREMIUM SILICONA REGULAR PUTTY SOFT 250+250 ml
- PRONTO DENTAL ADICION LIGHT 2 - 2x50 ml +12 MIX
- PRONTO DENTAL ADICION PUTTY 2 FAST - 250+250 ml
- SCHMIDT LINE REGISTRO DE MORDIDA 2x50 ml +12 MIXING TIPS
- VENTURA BITE 2.0 (2X50 ml)
- VENTURA IMPRESS 2.0 LIGHT BODY REGULAR SET (2X50 ml)
- VENTURA IMPRESS 2.0 PUTTY SOFT REGULAR SET (2x250 ml)
- VENTURA TOP 2.0 CATALYST – 60 ml
Showing 12 of 29 declared devices.
Catalogue references include 2133, 3142, 3166, 3176, 3212, 3387.
European nomenclature codes declared: Q01020104, Q01020101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 29 |
| Country of registration | Spain |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 29 |
|---|---|
| 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. MADESPA, S.A. was not found in either the U.S. or the Canadian register.