ZYLLION, INC.

FDA Device Registration & Listing · Lake Forest, CA, US · Registration 3009225484

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
3009225484
FEI Number
3009225484
Entity Name
ZYLLION, INC.
City/State/Country
Lake Forest, CA, US
Establishment Address
26439 Rancho Pkwy S, Unit 175, Lake Forest, CA 92630, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Zyllion, Inc. (Owner Number: 10045182)
Owner / Operator Contact Address
26439 Rancho Pkwy South, Unit 175, 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

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2013-10-31

Official Correspondent

Paul Hsu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Zyllion, Inc.
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 3009225484. Last updated year: 2026. Please use registration number 3009225484 when referencing this establishment in official correspondence.
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