Data / Medical devices / Israel / CMT Medical Technologies, Ltd.
CMT Medical Technologies, Ltd.: FDA-registered device maker in YOKNEAM ILLIT Northern, Israel, 4 510(k) clearances
CMT Medical Technologies, Ltd. is registered with the FDA (registration 8030112) in YOKNEAM ILLIT Northern, Israel. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated September 3, 2020. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 8030112
- FEI number
- 3005116291
- Address
- Hacarmel ST Building 7/2 P.O.B. 111, YOKNEAM ILLIT Northern, Israel, 20692
- Owner or operator
- CMT MEDICAL TECHNOLOGIES, LTD. (9011219)
- Roles
- Manufacturer
- First device listed
- April 12, 2011
- Registered through
- 2027
- Brand names listed
- ArtPIX DRF, ArtPix Mobile EZ2GO, DUET DRF, PrestoDR 3543EZ, PrestoDR 4143, PrestoDR 4343, PrestoDR Portable 3543
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Solid State X-Ray Imager (Flat Panel/Digital Imager) | MQB | 2 | Manufacturer | accessdata.fda.gov |
| System, X-Ray, Fluoroscopic, Image-Intensified | JAA | 2 | Manufacturer | accessdata.fda.gov |
| System, X-Ray, Stationary | KPR | 2 | 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 |
|---|---|---|---|---|---|---|
| September 3, 2020 | K202235 | ArtPIX DRF | JAA | Substantially Equivalent | Cmt Medical Technologies, Ltd. | accessdata.fda.gov |
| September 22, 2016 | K162224 | ArtPix Mobile EZ2GO | KPR | Substantially Equivalent | Cmt Medical Technologies, Ltd. | accessdata.fda.gov |
| April 26, 2011 | K110849 | PRESTODR 4143 | KPR | Substantially Equivalent | Cmt Medical Technologies, Ltd. | accessdata.fda.gov |
| March 29, 2011 | K103038 | DUET DRF | JAA | Substantially Equivalent | Cmt Medical Technologies, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Solid State X-Ray Imager (Flat Panel/Digital Imager)
- All makers of System, X-Ray, Stationary
- All makers of System, X-Ray, Fluoroscopic, Image-Intensified
Updated September 3, 2020. 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.