RECOVERY FORCE HEALTH

FDA Device Registration & Listing · Fishers, IN, US · Registration 3011118518

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3011118518
FEI Number
3011118518
Entity Name
RECOVERY FORCE HEALTH
City/State/Country
Fishers, IN, US
Establishment Address
10022 Lantern Rd Ste 100, Fishers, IN 46037, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Recovery Force Health (Owner Number: 10046926)
Owner / Operator Contact Address
10022 Lantern Rd, Suite 100, Fishers, IN 46037, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Movement and Compressions System, MAC System ELEVATE Patient Positioners

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOW Sleeve, Limb, Compressible Cardiovascular Class 2 870.5800 2021-03-30
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 2023-08-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Recovery Force Health
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K170216 Tactile Systems Technology, Inc. (Dba Tactile Medical) Flexitouch System 2017-05-26
K100306 Covidien KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES 2010-05-04

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3014834638 ZENITH TECHNICAL INNOVATIONS, LLC Gurnee, IL, US
3009155917 GRANDWAY TECHNOLOGY (SHENZHEN) LIMITED Shenzhen Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011118518. Last updated year: 2026. Please use registration number 3011118518 when referencing this establishment in official correspondence.
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