ALTIMATE MEDICAL, INC.
2 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (2)
- Inspections (2)
Devices registered here (1)
- Chair, Positioning, ElectricProduct code INO (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.3110
Recalls & enforcement
- Class IITerminated2022-11-30Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.
- Class IITerminated2022-10-04Some EasyStand Bantam Small and Extra Small standers with the non-supine option may have been manufactured with a component that affects the operation of the leg assembly bracket to maintain the standers non-supine position.
FDA inspections (2)
- NAI2025-05-22No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- NAI2017-11-15No Action Indicated · Compliance: Devices
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “ALTIMATE MEDICAL, INC. (FEI 2183634) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2183634-altimate-medical-inc/
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