LIFE RECOVERY SYSTEMS HD, LLC.

FDA Device Registration & Listing · Kinnelon, NJ, US · Registration 3006059109

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
3006059109
FEI Number
3006059109
Entity Name
LIFE RECOVERY SYSTEMS HD, LLC.
City/State/Country
Kinnelon, NJ, US
Establishment Address
170 Kinnelon Rd, Kinnelon, NJ 07405, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LIFE RECOVERY SYSTEMS HD, LLC. (Owner Number: 9095304)
Owner / Operator Contact Address
170 Kinnelon Rd, Kinnelon, NJ 07405, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K061023
PMA Number
N/A

All Registered Proprietary Names

THERMOSUIT SYSTEM

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NZE Hyperthermia Monitor Cardiovascular Class 2 870.5900 2006-12-05

Official Correspondent

ROBERT SCHOCK, PHD

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LIFE RECOVERY SYSTEMS HD, LLC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006059109. Last updated year: 2026. Please use registration number 3006059109 when referencing this establishment in official correspondence.
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