AVEERA MEDICAL

FDA Device Registration & Listing · San Clemente, CA, US · Registration 3027735872

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
3027735872
FEI Number
3027735872
Entity Name
AVEERA MEDICAL
City/State/Country
San Clemente, CA, US
Establishment Address
929 Calle Negocio Ste A, San Clemente, CA 92673, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Aveera Medical (Owner Number: 10093798)
Owner / Operator Contact Address
929 Calle Negocio, Suite A, San Clemente, CA 92673, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K250105
PMA Number
N/A

All Registered Proprietary Names

Boomerang

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MGZ Valvulotome Cardiovascular Class 2 870.4885 2025-07-11

Official Correspondent

Christopher Chapek

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aveera Medical
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 3027735872. Last updated year: 2026. Please use registration number 3027735872 when referencing this establishment in official correspondence.
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