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Thrive Orthopedics

Thrive Orthopedics LLC · Model F5 Magnetic AFO Xtra Small Right · UDI-DI 00810079190362

IQI Prescription
10
510(k) clearances
456
Adverse events (2 deaths)
17
Recalls
519
Facilities

Description

F5 AFO Dynamic Feedback Magnetic Spiral Ankle Foot Orthosis Xtra Small Right

Recalls

DateFirmReason
2023-09-23Townsend DesignDue to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
2023-09-23Townsend DesignDue to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
2023-09-23Townsend DesignDue to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
2018-01-313M Company - Health Care Business3M discovered that the Futuro" Quick Strap Ankle Brace (Cat. #47736EN) and ACE" Brand Deluxe Ankle brace (Cat. #207736) do not have the correct labeling. The products contain natur
2018-01-313M Company - Health Care Business3M discovered that the Futuro" Quick Strap Ankle Brace (Cat. #47736EN) and ACE" Brand Deluxe Ankle brace (Cat. #207736) do not have the correct labeling. The products contain natur
2016-11-07DeRoyal Industries IncDeRoyal received complaints of mold on Tennis Elbow Straps.
2016-11-07DeRoyal Industries IncDeRoyal received complaints of mold on Tennis Elbow Straps.
2016-02-24Ossur H / FOssur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve Gray, NecLoc Extrication Collar, Rebound Cartilage, Rebound Cartilage Custom, Rebound Air Walker, Rebound
2016-02-24Ossur H / FOssur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve Gray, NecLoc Extrication Collar, Rebound Cartilage, Rebound Cartilage Custom, Rebound Air Walker, Rebound
2016-02-24Ossur H / FOssur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve Gray, NecLoc Extrication Collar, Rebound Cartilage, Rebound Cartilage Custom, Rebound Air Walker, Rebound

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.