Pollogen Ltd
Active in EUDAMEDIsraelfrom SRN EUDAMED FDA SRN IL-MF-000031034 FEI 3008753275
Pollogen Ltd is a medical device manufacturer based in Israel, with 77 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II; EU Class IIa and IIb) as of 13 Nov 2026.
- Devices
- 77
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 47
- EUDAMED 27
- FDA 510(k) 18
- Device classes
- FDA Class II 62
- EU Class IIa 9
- EU Class IIb 6
- Top EMDN categories
- Sites and related companies
- Obelis S.A. authorised representative
- Identifiers
- EUDAMED SRN IL-MF-000031034
- FDA FEI 3008753275
- DUNS 514905681
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
- Authorised rep.
- Obelis S.A.BE
What Pollogen Ltd makes
Pollogen Ltd manufactures radio-frequency based skin and body contouring systems, including applicator tips, control units, and hybrid energy disposable tips for surface treatment and fat liquefaction. Their product line includes devices such as the Legend Pro, STOP VX MODEL U, triFX, TriLift, and STOP X, which are designed for non-invasive aesthetic procedures using radio-frequency technology.
The company's devices are classified as Class II, Class IIa, and Class IIb medical devices and are listed in regulatory databases including Eudamed, FDA 510(k), and FDA UDI. Pollogen Ltd is based in Israel (IL).
Catalogue
Search and filter all 77 devicesShowing 1-50 of 77
Company details
- EUDAMED SRN
- IL-MF-000031034
- FDA FEI number
- 3008753275
- DUNS number
- 514905681
- EUDAMED status
- Active
- EUDAMED registered name
- Pollogen Ltd
- Registered address
- 6, Kaufman st. Gibor House, 6801298, Tel-Aviv, Israel
- info@pollogen.com
- Phone
- +972-3-5104110
- PRRC contact
- Michal Borger
Frequently asked questions
How many devices does POLLOGEN LTD have in the registry?
The registry currently lists 77 devices for POLLOGEN LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list POLLOGEN LTD's devices?
Among its 50 most recently registered devices, POLLOGEN LTD has devices listed in EUDAMED (19 devices) and FDA GUDID (45 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do POLLOGEN LTD's devices fall under?
Among its 50 most recently registered devices, the classes recorded for POLLOGEN LTD's devices are Class IIa, Class IIb and Class II. Each device page shows its own class and authorisation.
What are the newest devices from POLLOGEN LTD in the registry?
The most recently registered devices listed for POLLOGEN LTD include gen XL2, gen XL3, Maximus Pro and triLift.