KARL STORZ Endoscopy-America, Inc.

KARL STORZ Endoscopy-America, Inc. holds 362 FDA 510(k) medical device clearances, first cleared 1980, most recent 2026, with 17 FDA device recalls on record.

Clearances by KARL STORZ Endoscopy-America, Inc. — page 4

301–362 of 362

Data sourced from openFDA. This site is unofficial and independent of the FDA.