Data / Medical devices / United States / Liger Medical
Liger Medical: FDA-registered device maker in Lehi, UT, United States, 3 510(k) clearances
Liger Medical is registered with the FDA (registration 3009903460) in Lehi, UT, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 23, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009903460
- Address
- 3300 North Running Creek Way Building G, Basement Suite G20, Lehi, UT, United States, 84043
- Owner or operator
- Liger Medical (10048911)
- Roles
- Manufacturer
- First device listed
- March 18, 2015
- Registered through
- 2026
- Brand names listed
- ESU-110 Electrosurgery Generator, EVA Pro Digital Colposcope, HTU-110 ThermoCoagulator, IRIS, MobileODT ThermoGlide Thermocoagulation Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Colposcope (And Colpomicroscope), Exempt | PTZ | 2 | Manufacturer | accessdata.fda.gov |
| Electrocautery, Gynecologic (And Accessories) | HGI | 2 | Manufacturer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 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 |
|---|---|---|---|---|---|---|
| April 23, 2021 | K202915 | IRIS Thermocoagulator and Digital Colposcope | HGI | Substantially Equivalent | Liger Medical, LLC | accessdata.fda.gov |
| June 24, 2016 | K152843 | Liger Medical HTU-110 | HGI | Substantially Equivalent | Liger Medical, LLC | accessdata.fda.gov |
| February 12, 2014 | K133273 | LIGER MEDICAL ESU-110 | GEI | Substantially Equivalent | Liger Medical, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Electrocautery, Gynecologic (And Accessories)
- All makers of Colposcope (And Colpomicroscope), Exempt
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
Updated April 23, 2021. 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.