Leica Microsystems (Schweiz) AG
Leica Microsystems (Schweiz) AG holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2019, with 2 FDA device recalls on record.
Top product codes for Leica Microsystems (Schweiz) AG
FDA recalls by Leica Microsystems (Schweiz) AG
- Z-2177-2013 — Surgical microscope The device is used to improve the visibility of objects through magnification and illumination and can be applied for observation and documentation and for human veterinary medical treatment.
- Z-2176-2013 — Surgical microscope The device is used to improve the visibility of objects through magnification and illumination and can be applied for observation and documentation and for human veterinary medical treatment.
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 Leica Microsystems (Schweiz) AG
Data sourced from openFDA. This site is unofficial and independent of the FDA.