ACTIVEWRAP

FDA Device Registration & Listing · Lake Forest, CA, US · Registration 3007886350

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
3007886350
FEI Number
3007886350
Entity Name
ACTIVEWRAP
City/State/Country
Lake Forest, CA, US
Establishment Address
26439 Rancho Pkwy S Ste 150, Lake Forest, CA 92630, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ActiveWrap (Owner Number: 10030125)
Owner / Operator Contact Address
26439 Rancho Pkwy, Ste 150, Lake Forest, CA 92630, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BAWP004 BAWP003 COLD710 COLD1310 BAWP005 COLD1010 BAWP006 BAWP007

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2013-04-22

Official Correspondent

Tyler Hardy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ActiveWrap
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 3007886350. Last updated year: 2026. Please use registration number 3007886350 when referencing this establishment in official correspondence.
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