Medical Device Manufacturer · US , St. Louis , MO

Storz - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1992

6

Total

6

Cleared

0

Denied

Storz has 6 FDA 510(k) cleared medical devices. Based in St. Louis, US.

Historical record: 6 cleared submissions from 1992 to 1996. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Storz Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Storz

6 devices

1-6 of 6

Cleared Mar 26, 1996

STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR

Ophthalmic · 84d

Cleared Mar 04, 1996

STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND...

Ophthalmic · 301d

Cleared Dec 14, 1995

STORZ MICROFLOW PHACOEMULSIFICATION NEEDLE

Ophthalmic · 87d

Cleared Feb 09, 1994

STORZ COMPUSCAN AB

Radiology · 384d

Cleared Sep 09, 1993

STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE

Ophthalmic · 253d

Cleared Feb 21, 1992

STORZ MICRO CUTTER 25 GAUGE PACK

Ophthalmic · 198d