Medical Device Manufacturer · CH , Port

Sie Ag,Surgical Instrument Engineering - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015
2
Total
2
Cleared
0
Denied

Sie Ag,Surgical Instrument Engineering has 2 FDA 510(k) cleared medical devices. Based in Port, CH.

Last cleared in 2022. Active since 2015. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Sie Ag,Surgical Instrument Engineering Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Insight, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Sie Ag,Surgical Instrument Engineering
2 devices
1-2 of 2
Cleared Apr 21, 2022
FEMTO LDV Z8 Femtosecond Surgical Laser
K213559 · OOE
Ophthalmic · 168d
Cleared Oct 23, 2015
FEMTO LDV Z8 Surgical Laser
K150323 · OOE
Ophthalmic · 256d
Filters
Filter by Specialty
All2 Ophthalmic 2