Avita Medical Americas LLC

FDA Device Registration & Listing · Ventura, CA, US · Registration 2029412

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
2029412
FEI Number
3001452123
Entity Name
Avita Medical Americas LLC
City/State/Country
Ventura, CA, US
Establishment Address
3007 Bunsen Ave, UNIT K, Ventura, CA 93003, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Avita Medical Americas LLC (Owner Number: 10058722)
Owner / Operator Contact Address
28159 Avenue Stanford, Suite 220, Valencia, CA 91355, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
BP220799

All Registered Proprietary Names

RECELL RECELL GO mini RECELL GO PermeaDerm B, C and G RECELL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QCZ Mechanical And Enzymatic Autologous Skin Processor For Cell Suspension, With Applicator Unknown Class 3 N/A 2018-10-23
FRO Dressing, Wound, Drug Unknown Class U N/A 2025-05-22
QWY Mechanical And Enzymatic Autologous Skin Processor For Cell Suspension, For Stable Vitiligo, With Applicator Unknown Class 3 N/A 2023-06-29

Official Correspondent

Ron Lagerquist

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Avita Medical Americas LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3014270795 AVITA MEDICAL AMERICAS LLC Valencia, CA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K150256 Argentum Medical SILVERLON BURN CONTACT DRESSINGS 2015-04-30

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-06 B. Braun Medical, Inc. U
D-Stat Dry Hemostatic Bandage. The product is an adhesive bandage.
Z-0038-2025 3M Company Health Care Business 3m Center U
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R

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3014270795 AVITA MEDICAL AMERICAS LLC Valencia, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2029412. Last updated year: 2026. Please use registration number 2029412 when referencing this establishment in official correspondence.
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