Data / Medical devices / Israel / Carevature Technologies Ltd
Carevature Technologies Ltd: FDA-registered device maker in Netanya Central, Israel, 1 510(k) clearance
Carevature Technologies Ltd is registered with the FDA (registration 3030956508) in Netanya Central, Israel. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 16, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030956508
- Address
- 31 Yad Harutzim Street, Netanya Central, Israel, 4250529
- Owner or operator
- Carevature Technologies LTD (10090517)
- Roles
- Manufacturer
- First device listed
- April 8, 2024
- Registered through
- 2026
- Brand names listed
- Dreal® B3S45FI, Dreal® B3S45FU, Dreal® B3S45FUS, Dreal® C2L75FU, Dreal® C3B10ML, Dreal® C3L10DS, Dreal® C3S10ML, Dreal® C3S45FI and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Drills, Burrs, Trephines & Accessories (Simple, Powered) | HBE | 2 | Manufacturer | accessdata.fda.gov |
| Motor, Surgical Instrument, Pneumatic Powered | GET | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 16, 2016 | K153519 | DReal | HBE | Substantially Equivalent | Carevature Medical, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Drills, Burrs, Trephines & Accessories (Simple, Powered)
- All makers of Motor, Surgical Instrument, Pneumatic Powered
Updated March 16, 2016. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.