Ellipse A/S
Ellipse A/S holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2020, with 2 FDA device recalls on record.
Top product codes for Ellipse A/S
FDA recalls by Ellipse A/S
- Z-1697-2016 — Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser Products.
- Z-1698-2016 — Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Laser Products.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Ellipse A/S
- K192951 — Ellipse Frax 1940 for Ellipse Nordlys and Ellipse Ydun
- K180406 — Ellipse Ydun
- K161162 — Frax 1550 for Ellipse Nordlys/ Ellipse Nordlys+, Ellipse Sirius, Ellipse Infinity, Ellipse Mjolner, Ellipse Nordlys Ultra
- K150907 — Ellipse Nordlys/Ellipse Nordlys+, Ellipse Sirius, Ellipse Infinity, Ellipse Mjolner, Ellipse Nordlys Ultra
- K140670 — ELLIPSE I2PL+/ELLIPSE MULTIFLEX+
- K081408 — ELLIPSE MULTIFLEX
- K072023 — ELLIPSE JUVIA, MODEL 9EJU7465
Data sourced from openFDA. This site is unofficial and independent of the FDA.