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Data / Medical devices / United States / Recovery Force Health

Recovery Force Health: FDA-registered device maker in Fishers, IN, United States, 1 510(k) clearance

Recovery Force Health is registered with the FDA (registration 3011118518) in Fishers, IN, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 21, 2021. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3011118518
Address
10022 Lantern Rd Ste 100, Fishers, IN, United States, 46037
Owner or operator
Recovery Force Health (10046926)
Roles
Complaint file establishment, Manufacturer, Specification developer
First device listed
March 30, 2021
Registered through
2026
Brand names listed
ELEVATE Patient Positioners, Movement and Compressions System, MAC System

Devices it lists

DeviceProduct codeClassRoleSource
Protector, Skin PressureFMP1Complaint file establishment, Specification developeraccessdata.fda.gov
Sleeve, Limb, CompressibleJOW2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
March 21, 2021K203052Movement and Compressions System (the MAC System)JOWSubstantially EquivalentRecovery Force, LLCaccessdata.fda.gov

Compare with other makers

Updated March 21, 2021. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.