Data / Medical devices / Israel / Vibrant Ltd
Vibrant Ltd: FDA-registered device maker in Yokne'am Illit Haifa, Israel, 1 510(k) clearance
Vibrant Ltd is registered with the FDA (registration 3025305436) in Yokne'am Illit Haifa, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 26, 2022. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3025305436
- Address
- Hacarmel St. 2, Yokne'am Illit Haifa, Israel, 2069206
- Owner or operator
- Vibrant LTD (10086670)
- Roles
- Manufacturer
- First device listed
- December 4, 2022
- Registered through
- 2027
- Brand names listed
- Vibrant System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Orally Ingested Transient Device For Constipation | QTN | 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 26, 2022 | DEN210052 | Vibrant System | QTN | Unknown | Vibrant, Ltd. | accessdata.fda.gov |
Updated August 26, 2022. 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.