Richard Wolf GmbH is one of 387 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Richard Wolf GmbH - FDA 510(k) Cleared Devices
Recent clearances: MINIATURE LAPAROSCOPE SET (MINI LAP)
1
Total
1
Cleared
0
Denied
Richard Wolf GmbH, is a medical device manufacturer specializing in endoscopic instruments and minimally invasive surgical systems. The company operates with a manufacturing facility in Knittlingen, Baden-Württemberg, Germany, and maintains a global presence across multiple continents.
Richard Wolf GmbH received 1 FDA 510(k) clearance from 1 total submission in the General & Plastic Surgery category. The clearance was granted in 1996 for a miniature laparoscope set. The company has been inactive in FDA submissions for more than five years and should be treated as a historical regulatory record.
Founded in 1947, Richard Wolf established itself as a pioneer in endoscopic technology, introducing innovations such as cold-light illumination, modern rod-lens optics, and extracorporeal shock wave lithotripsy systems. The company expanded internationally beginning in the 1970s, establishing subsidiaries across Europe, North America, and Asia.
Explore the complete regulatory history, device names, product codes, and clearance dates in the database records below.
FDA 510(k) Regulatory Record - Richard Wolf GmbH
1 devices