Data / Medical devices / Israel / Samsara Vision Ltd.
Samsara Vision Ltd.: FDA-registered device maker in Petah Tikva Central, Israel, 1 PMA approval
Samsara Vision Ltd. is registered with the FDA (registration 3005347768) in Petah Tikva Central, Israel. It lists 2 device types. The FDA files 1 PMA approval under its listings, the newest dated July 1, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005347768
- Address
- 21 Yegia Kapayim ST., Petah Tikva Central, Israel, 4913020
- Owner or operator
- Samsara Vision Inc. (9079659)
- Roles
- Manufacturer
- First device listed
- February 13, 2006
- Registered through
- 2026
- Brand names listed
- SING External Miniature Telescope Handheld Piece, SING Implantable Miniature Telescope
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Telescope, Hand-Held, Low-Vision | HKB | 1 | Manufacturer | accessdata.fda.gov |
| Telescope, Implantable, Miniature | NCJ | 3 | Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| July 1, 2010 | P050034 | IMPLANTABLE MINIATURE TELESCOPE (IMT) | NCJ | 20 | December 17, 2024 | accessdata.fda.gov |
Compare with other makers
Updated December 17, 2024. 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.