Data / Medical devices / Israel / Medoc Ltd.
Medoc Ltd.: FDA-registered device maker in RAMAT YISHAI Northern, Israel, 3 510(k) clearances
Medoc Ltd. is registered with the FDA (registration 8044062) in RAMAT YISHAI Northern, Israel. It lists 5 device types. The FDA files 3 510(k) clearances under its listings, the newest dated January 19, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8044062
- FEI number
- 3005773477
- Address
- 1 HaDekel Street, RAMAT YISHAI Northern, Israel, 3009500
- Owner or operator
- MEDOC LTD. ADVANCED MEDICAL SYSTEMS (9005342)
- Roles
- Manufacturer
- First device listed
- July 23, 2001
- Registered through
- 2026
- Brand names listed
- AlgoMed FPIX, CHEPS, Pathway, Q-Sense, TSA 2, TSA 2 Air, VSA 2, VSA-3000
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Vibration Threshold Measurement | LLN | 1 | Manufacturer | accessdata.fda.gov |
| Dynamometer, Nonpowered | HRW | 1 | Manufacturer | accessdata.fda.gov |
| Evoked Potential Stimulator, Thermal | NTU | 2 | Manufacturer | accessdata.fda.gov |
| Test, Temperature Discrimination | LQW | 1 | Manufacturer | accessdata.fda.gov |
| Vibrator, Therapeutic | IRO | 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 |
|---|---|---|---|---|---|---|
| January 19, 2006 | K052357 | PATHWAY - ATS/CHEPS | NTU | Substantially Equivalent | Medoc Ltd. Advanced Medical Systems | accessdata.fda.gov |
| April 25, 1997 | K970180 | VSA 3000 VIBRATORYN SENSORY ANALYZER | LLN | Substantially Equivalent | Eare Consulting Service | accessdata.fda.gov |
| October 21, 1993 | K922052 | TSA 2001 THERMAL SENSORY ANALYZER | LQW | Substantially Equivalent | Medoc Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Dynamometer, Nonpowered
- All makers of Test, Temperature Discrimination
- All makers of Vibrator, Therapeutic
- All makers of Device, Vibration Threshold Measurement
Updated January 19, 2006. 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.