Speculum, Vaginal, Metal
FDA product code HDF · Class 1 · 14 devices · 48 reports · 10 devices named in recalls
- V. Mueller GL11Steris Corporation · SPECULUM, VAGINAL, METAL1 recall1 report
- Sklar Instruments 96-2603Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar Instruments 96-2605Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar Instruments 96-2613Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar Instruments 96-2615Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar Instruments 96-2616Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar Instruments 96-2617Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- V. Mueller GL31Steris Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar® 96-2607Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar® 96-3001Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Millennium 1-70542Avalign Technologies, Inc. · Speculum, Vaginal, Metal38 reports
- Millennium 1-70551Avalign Technologies, Inc. · SPECULUM, VAGINAL, METAL7 reports
- Millennium 1-70543Avalign Technologies, Inc. · Speculum, Vaginal, Metal1 report
- Trinity Sterile, Inc. 22202Trinity Sterile, Inc. · SPECULUM, VAGINAL, METAL1 report