TRULIFE, INC.

FDA Device Registration & Listing · Jackson, MI, US · Registration 1812798

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
1812798
FEI Number
1812798
Entity Name
TRULIFE, INC.
City/State/Country
Jackson, MI, US
Establishment Address
2010 East High Street, Jackson, MI 49204, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Trulife, Inc. (Owner Number: 10027457)
Owner / Operator Contact Address
3225 Woburn Street, Suite 160, Bellingham, WA 98226, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HyperEx OrthoPro AirPro SoftPro DynaPro Bebax SpinAir

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2021-10-14
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2021-09-27
KNP Orthosis, Corrective Shoe Physical Medicine Class 1 890.3475 2021-10-14
IQE Orthosis, Lumbar Physical Medicine Class 1 890.3490 2021-10-14

Official Correspondent

Dannielle Rehbein

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Trulife, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1812798. Last updated year: 2026. Please use registration number 1812798 when referencing this establishment in official correspondence.
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