Corflex
United Statesfrom the FDA registration address FDA establishment FEI 1218997
- Devices
- 0
- Registrations
- FDA
- FDA recalls
- 7
Company details
- FDA FEI number
- 1218997
- Address
- 669 EAST INDUSTRIAL PARK, MANCHESTER, NH, 03109
FDA recalls
2015
- 12 Nov 2015 Z-0574-2016 Class II Terminated Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may occur at the affected knee joint,
- 12 Nov 2015 Z-0575-2016 Class II Terminated Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may occur at the affected knee joint,
- 12 Nov 2015 Z-0576-2016 Class II Terminated Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may occur at the affected knee joint,
- 12 Nov 2015 Z-0577-2016 Class II Terminated Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may occur at the affected knee joint,
- 12 Nov 2015 Z-0578-2016 Class II Terminated Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may occur at the affected knee joint,
- 12 Nov 2015 Z-0579-2016 Class II Terminated Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may occur at the affected knee joint,
- 12 Nov 2015 Z-0580-2016 Class II Terminated Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may occur at the affected knee joint,