Retractor
FDA product code GAD · Class 1 · 326 devices · 533 reports · 1 deaths reported · 171 devices named in recalls
- NA 03.809.900Synthes GmbH · RETRACTOR1 report
- NA 03.816.030Synthes GmbH · RETRACTOR1 report
- NA 03.816.037Synthes GmbH · RETRACTOR1 report
- NA 03.816.120Synthes GmbH · RETRACTOR1 report
- NA 03.816.320Synthes GmbH · RETRACTOR1 report
- SynFrame 387.451Synthes GmbH · RETRACTOR1 report
- SynFrame 387.452Synthes GmbH · RETRACTOR1 report
- V. Mueller SU3660Steris Corporation · RETRACTOR1 report
- Equinoxe 317-21-05Exactech, Inc. · RETRACTOR1 report
- NA SD398.003Synthes GmbH · RETRACTOR1 report
- NA 03.100.013Synthes GmbH · RETRACTOR1 report
- NA 03.100.014Synthes GmbH · RETRACTOR1 report
- NA 03.100.015Synthes GmbH · RETRACTOR1 report
- NA 03.100.016Synthes GmbH · RETRACTOR1 report
- NA 03.100.017Synthes GmbH · RETRACTOR1 report
- NA 03.100.112Synthes GmbH · RETRACTOR1 report
- NA 03.100.119Synthes GmbH · RETRACTOR1 report
- NA 03.401.054Synthes GmbH · RETRACTOR1 report
- NA 399.197Synthes GmbH · RETRACTOR1 report
- NA 399.21Synthes GmbH · RETRACTOR1 report
- NA 399.25Synthes GmbH · RETRACTOR1 report
- NA 03.164.008Synthes GmbH · RETRACTOR1 report
- NA 03.164.012Synthes GmbH · RETRACTOR1 report
- Fathom MR2-102075Seaspine Orthopedics Corporation · RETRACTOR1 report
- V. Mueller OS8818-23Steris Corporation · RETRACTOR1 report
- Superpath 20071004Microport Orthopedics Inc. · RETRACTOR1 report