Hdc S.r.l.
Country not established FDA
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Hdc S.r.l. makes
Hdc S.R.L. manufactures orthopedic fixation devices, including the HDC Spider Screw, a threaded implant for bone stabilization, and sterile variants such as the HDC Sterile Spider Screw and the self-ligating HDC Sterile Self Ligating Spider Screw (models SLI, SL2). These products are designed for surgical applications requiring secure bone attachment.
The company’s portfolio is classified under FDA Class II devices and is listed via 510(k) clearance in the United States. The manufacturer is based in the US.
Catalogue
Hdc Spider Screw Ref K052471
Regimes: 510(k) Registry: 510(k)Hdc Sterile Spider Screw Ref K071851
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
FDA establishments
- Hdc S.R.L. THIENE Vicenza · IT FEI 3005728057
Frequently asked questions
How many devices does Hdc S.R.L. have in the registry?
The registry currently lists 3 devices for Hdc S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hdc S.R.L.'s devices?
Among its 3 most recently registered devices, Hdc S.R.L. has devices listed in FDA 510(k) (3 devices).
What risk classes do Hdc S.R.L.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Hdc S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hdc S.R.L. in the registry?
The most recently registered devices listed for Hdc S.R.L. include HDC SPIDER SCREW, HDC STERILE SPIDER SCREW and HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI, SL2.
Which FDA establishments are linked to Hdc S.R.L.?
1 FDA establishment is linked to Hdc S.R.L. in the registry; they are listed on the company page.