Aliya PEF Ablation Pack

Aliya PEF Ablation Pack, 5 Pack and 1 Pack

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (3), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code OAB
Manufacturer City Province Registered as Device types
Energenx Medical Ltd. Shanghai Shanghai Contract manufacturer 2
Jiana Sterilization Technology (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 23
Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. Cixi Zhejiang Manufacturer 8
Zhejiang Curaway Medical Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7

Record

Regulatory record for Aliya PEF Ablation Pack
Listed by Galvanize Therapeutics, United States
FDA product code OAB
Device type Low Energy Direct Current Thermal Ablation System
Device class Class 2
Regulation 21 CFR 878.4400
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K212871
Record published 2026-05-14

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date
Packaging Box, box of 5

Catalogue Numbers

Catalogue numbers for Aliya PEF Ablation Pack
Catalogue number Size Status
GTI-00050 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Curaway Zhejiang Curaway Medical Technology Co., Ltd. 25
NanoKnife AngioDynamics, Inc. 25
Dophi Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. 8
Aliya Needle Galvanize Therapeutics 2
Aliya Generator Galvanize Therapeutics 1
Aliya Electrode Galvanize Therapeutics 1
US Medical Innovations US Medical Innovations, LLC 1
Aliya Generator-Recertified Galvanize Therapeutics 1
Inumi Flex Needle Galvanize Therapeutics 1
Inumi Flex Needle Pack Galvanize Therapeutics 1

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253826 2026-05-07
K233884 2024-05-22
K212871 2022-06-17

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer