Amron International, Inc.

FDA Device Registration & Listing · Vista, CA, US · Registration 1000280680

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
1000280680
FEI Number
1000280680
Entity Name
Amron International, Inc.
City/State/Country
Vista, CA, US
Establishment Address
1380 Aspen Way, Vista, CA 92081, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Amron International, Inc (Owner Number: 10028802)
Owner / Operator Contact Address
1380 Aspen Way, Vista, CA 92081, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Amron Oxygen Treatment Hood

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FOG Hood, Oxygen, Infant Anesthesiology Class 1 868.5700 2018-08-16

Official Correspondent

David Lynch

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Amron International, 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 1000280680. Last updated year: 2026. Please use registration number 1000280680 when referencing this establishment in official correspondence.
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