Tecres S.p.A.
Active in EUDAMEDItalyfrom SRN EUDAMED SRN IT-MF-000027512
- Devices
- 87
- Registrations
- EUDAMED
At a glance
EU certificates
8 of 8 in force.
Market reach
- European Union
- EUDAMED actor, 8 certificates
What Tecres S.p.A. makes
Tecres S.p.A. manufactures orthopedic and spinal fixation devices, including temporary joint spacers for the hip and shoulder, such as the InterSpace GV Hip Spacer and SPACER-S Shoulder Spacer. Their portfolio also includes bone cements (e.g., Bone Cement Genta, KYPHON VuE) and spinal systems like the Mendec Kypho Set and MENDEC SPINE delivery kits. Additional products cover knee prostheses, including the InterSpace Knee range, and specialized components for surgical procedures in orthopedics.
The company’s devices are classified under EU Medical Device Regulations as Class II and Class IIa, with listings in the EU’s eudamed database and FDA’s 510(k) premarket notification registry. These products are intended for use in orthopedic and spinal surgeries, adhering to regulatory requirements for temporary implants, bone fixation, and joint reconstruction. Tecres S.p.A. is based in Italy.
Catalogue
Search and filter all 87 devicesShowing 1-50 of 87
Company details
- EUDAMED SRN
- IT-MF-000027512
- SRN (system / procedure pack)
- IT-PR-000027511
- EU VAT number
- IT02042700233
- EUDAMED status
- Active
- EUDAMED registered name
- Tecres S.p.A.
- Registered address
- 6, Via Andrea Doria, 37066, Sommacampagna, Italy
- Website
- www.tecres.it
- [email protected]
- Phone
- +39 045 9217311
- PRRC contact
- Giuseppe Gazzara
EUDAMED certificates
8 certificates8 valid, 0 expiredMDR 8next expiry 16 Jan 2028
BSI Group The Netherlands B.V. 2797 8 certificates
- MDR 773665 Active
Technical documentation EU MDR
- Issued
- 19 Feb 2026
- Expires
- 4 Nov 2030
- Reason
- Other
- MDR 739357 Active
Technical documentation EU MDR
- Issued
- 19 Feb 2026
- Expires
- 28 May 2030
- Reason
- Other
- MDR 739370 Active
Technical documentation EU MDR
- Issued
- 17 Nov 2023
- Expires
- 16 Nov 2028
- MDR 738100 Active
Technical documentation EU MDR
- Issued
- 19 Feb 2026
- Expires
- 16 Jan 2028
- Reason
- Other
- MDR 738108 Active
Technical documentation EU MDR
- Issued
- 10 Dec 2025
- Expires
- 16 Jan 2028
- Reason
- Other
- MDR 738112 Active
Technical documentation EU MDR
- Issued
- 19 Feb 2026
- Expires
- 16 Jan 2028
- Reason
- Other
- MDR 739361 Active
Technical documentation EU MDR
- Issued
- 10 Dec 2025
- Expires
- 16 Jan 2028
- Reason
- Other
- MDR 739363 Active
Technical documentation EU MDR
- Issued
- 17 Jan 2023
- Expires
- 16 Jan 2028
Frequently asked questions
How many devices does Tecres S.p.A. have in the registry?
The registry currently lists 87 devices for Tecres S.p.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tecres S.p.A.'s devices?
Among its 50 most recently registered devices, Tecres S.p.A. has devices listed in EUDAMED (50 devices).
What risk classes do Tecres S.p.A.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Tecres S.p.A.'s devices are Class I, Class IIa and Class III. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Tecres S.p.A.?
EUDAMED lists 8 certificates for Tecres S.p.A. (technical documentation) under MDR. 2 are recorded with the status issued. The most recent was issued on 19 Feb 2026.
What are the newest devices from Tecres S.p.A. in the registry?
The most recently registered devices listed for Tecres S.p.A. include SPACER-G FLAT 46 XL, MECTACEM-X HV WITH GENTAMICIN, VANCOGENX-SPACE KNEE 8074 and VANCOGENX-SPACE KNEE 6054.