Tecres
Country not established FDA
Tecres is a medical device manufacturer, with 114 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I) as of 12 Nov 2026.
- Devices
- 114
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 113
- EUDAMED 44
- FDA 510(k) 1
- Device classes
- FDA Class II 68
- FDA Class I 46
At a glance
Market reach
- United States
- FDA establishment
What Tecres makes
Tecres manufactures orthopaedic cement preparation and delivery systems, including kits for mixing and injecting bone cement, as well as antimicrobial and non-antimicrobial cement formulations. Their portfolio also includes bone access cannulas, cement spacers for joint revisions, trial prostheses for hip replacements, and polymer restrictors for controlling cement flow. Specific products include injection needles, cement restrictors, and systems like the InterSpace Hip Trial and Conflow G Bone Cement.
The company’s devices are regulated under FDA classifications, with most falling into Class I and Class II categories. Products are authorised via 510(k) clearances and listed in the FDA’s Unique Device Identifier (UDI) database. Tecres operates from the United States.
Catalogue
Search and filter all 114 devicesShowing 1-50 of 114
FDA establishments
- Tecres SpA VERONA Veneto · IT FEI 3002808402
Frequently asked questions
How many devices does Tecres have in the registry?
The registry currently lists 114 devices for Tecres. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tecres's devices?
Among its 50 most recently registered devices, Tecres has devices listed in EUDAMED (16 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Tecres's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Tecres's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tecres in the registry?
The most recently registered devices listed for Tecres include Mendec® Kypho Set Monolateral 10 mm ASB030A, Mendec® Kypho Set Monolateral 15 mm ASB030B, InterSpace Hip Trial, 60mm Short IHT60S and InterSpace Hip Trial, 54mm Short IHT54S.
Which FDA establishments are linked to Tecres?
1 FDA establishment is linked to Tecres in the registry; they are listed on the company page.