Dophi

Electroporation Fixator support

Registry build 21.09.26
4manufacturers in China registered for this device type
8catalogue numbers in this listing
1510(k) clearance

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 Dophi
Listed by Surgnova Healthcare Technologies (Zhejiang) Co., Ltd., China
FDA product code OAB
Device type Low Energy Direct Current Thermal Ablation System
Device class Class 2
Regulation 21 CFR 878.4400
Establishment Manufacturer
510(k) K240376
Record published 2026-05-22

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Dophi
Catalogue number Size Status
NSP13 In distribution
NSP18 In distribution
NTP13 In distribution
NFS06 In distribution
NSP25 In distribution
NTP25 In distribution
NTP18 In distribution
NPG3000 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
Aliya Needle Galvanize Therapeutics 2
Aliya Generator Galvanize Therapeutics 1
Aliya Electrode Galvanize Therapeutics 1
US Medical Innovations US Medical Innovations, LLC 1
Aliya PEF Ablation Pack Galvanize Therapeutics 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
K240376 2024-10-04

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