AZENA MEDICAL

FDA Device Registration & Listing · Walnut Creek, CA, US · Registration 3011877721

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
3011877721
FEI Number
3011877721
Entity Name
AZENA MEDICAL
City/State/Country
Walnut Creek, CA, US
Establishment Address
1777 Botelho Dr Ste 100, Walnut Creek, CA 94596, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Azena Medical (Owner Number: 10051175)
Owner / Operator Contact Address
1777 Bothelo Dr. Suite 100, Walnut Creek, CA 94596, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Gemini 810+980 Soft Tissue Laser Gemini NOVA Gemini EVO Gemini Diode Laser

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2016-02-11
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2026-03-26
NVK Laser, Dental, Soft Tissue General, Plastic Surgery Class 2 878.4810 2026-03-26
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2026-03-26
NVK Laser, Dental, Soft Tissue General, Plastic Surgery Class 2 878.4810 2021-12-14
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2021-12-14
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2021-12-14
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2020-03-06
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2020-03-06

Official Correspondent

Lindsay Tilton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K083258 Dornier Medtech America, Inc. MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE 2009-01-30
K201111 Candela Corporation GentleMax Pro Plus 2020-05-26
K202758 Shangdong Huamei Technology Co., Ltd. Nd: YAG Laser Therapy Systems HM-YL900 2020-11-16
K904068 Luxar Corp. LUXAR MODEL LX-20 CO2 LASER 1991-04-15
K142225 CAO Group, Inc. Pilot Elite Diode Laser 2014-09-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0005-2014 PhotoMedex, Inc. 2
The product is labeled in part "***Surgical Laser Technologies, Inc. Montgomeryville, PA***SLT Fiber Delivery System***Sterile***Non-Pyrogenic***. The product is packaged in a flexible pouch and includes the following laser surgery accessories - SLT-SSRH 8, Catalog/Product Number 0041-3082; SLT-SSRH 11, Catalog/Product Number 0041-3112; SLT-SSRH 4-SMA, Catalog/Product Number 0042-0075; SLT-SSRH 5-SMA, Catalog/Product Number 0042-0076; SLT-SSRH 6-SMA, Catalog/Product Number 0042-0077; SLT-SSRH 7-SMA, Catalog/Product Number 0042-0078; SLT-SSRH 8-SMA, Catalog/Product Number 0042-0079; SLT-SSRH 9-SMA, Catalog/Product Number 0041-4931; and SLT-SSRH 10-SMA, Catalog/Product Number 0042-0081. Indicated for the incision, excision, coagulations, and vaporization of soft tissue.
Z-0025-2018 Medtronic Navigation, Inc. 2
VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip; Part Number: 9735560 Visualase Cooled Laser Applicator System 10mm Tip; Part Number: 9735561 Visualase Cooled Laser Applicator System 15mm Tip
Z-0028-2007 Lumenis Inc. 2
Lumenis brand DuoTome SideLite 550 Micron Delivery System; laser systems for ablating soft tissue. Catalog Number: 0641-800-01; Manufactured by Lumenis, Inc., 2400 Condensa Street, Santa Clara, CA

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011877721. Last updated year: 2026. Please use registration number 3011877721 when referencing this establishment in official correspondence.
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