Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Blue Belt TechnologiesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Blue Belt Technologies MN with 4 device recalls. The most recent is a device recall dated Jun 4, 2014: Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Kne….
| Jun 4, 2014 | Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.Class II · Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains PFSI-00054, Right Medial/Left lateral impla | Device recalls |
| Jun 4, 2014 | Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.Class II · Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains PFSI-00054, Right Medial/Left lateral impla | Device recalls |
| Apr 11, 2014 | NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020.Class II · Blue Belt Technologies is conducting a voluntary recall for their Navio PFS system which is used during orthopedic knee | Device recalls |
| Jul 19, 2013 | Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product Usage: The intended use of this device is Class II · Blue Belt Technologies is recalling sterile Monitor Drapes used with their Navio PFS system during orthopedic knee surge | Device recalls |
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