Data / Medical devices / Israel / Cormed
Cormed: FDA-registered device maker in Bar-Lev Northern, Israel, 1 510(k) clearance
Cormed is registered with the FDA (registration 3030384100) in Bar-Lev Northern, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 17, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030384100
- Address
- 23 HaRotem Street, Bar-Lev Northern, Israel, 2015600
- Owner or operator
- CORMED (10089675)
- Roles
- Manufacturer
- First device listed
- December 27, 2023
- Registered through
- 2026
- Brand names listed
- Halo
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System | ONB | 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 |
|---|---|---|---|---|---|---|
| August 17, 2018 | K180574 | Halo Closed Vial Adaptor (Multiple Models based on 13, 20 or 28mm Vial Neck Size), Halo Closed Syringe Adaptor, Halo Closed Line Adaptor, Closed Vial Adaptor | ONB | Substantially Equivalent | J & J Solutions, Inc. D/B/A/ Corvida Medical | accessdata.fda.gov |
Compare with other makers
Updated August 17, 2018. 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.