RegWardenFDA facility compliance records
Facility

Altimate Medical, Inc.

2 recall(s) on record — most severe on record: Class II.

FDA Establishment Identifier (FEI)2126684
Establishment typeManufacture Medical Device
Location101 ACTIVEAID RD.
Redwood Falls, MN, US 56283
Registration statusActive · expires 2026
Parent companyAltimate Medical, Inc. (owner-operator 2126684)
Brand namesActiveAid SC; ActiveAid BCB; 600; 1100; 720; 285; 1218; 922; 202; 285TR; 101

Devices registered here (1)

Recalls & enforcement

Related

Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →

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