Richard Wolf Medical Instruments Corp.

Richard Wolf Medical Instruments Corp. holds 142 FDA 510(k) medical device clearances, first cleared 1977, most recent 2016, with 9 FDA device recalls on record.

Top product codes for Richard Wolf Medical Instruments Corp.

GCJ — Gastroenterology, Urology28 devices
HRX — Orthopedic14 devices
GEI — General, Plastic Surgery11 devices
HET — Obstetrics/Gynecology9 devices
HIF — Obstetrics/Gynecology7 devices
HIH — Obstetrics/Gynecology6 devices
FFK — Gastroenterology, Urology4 devices
GCT — Gastroenterology, Urology4 devices
FET — Gastroenterology, Urology3 devices
FGB — Gastroenterology, Urology3 devices

FDA recalls by Richard Wolf Medical Instruments Corp.

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 Richard Wolf Medical Instruments Corp.

1–100 of 142

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