Xstim

Xstim Electrode Cable, Short

Registry build 21.09.26
1manufacturer
11catalogue numbers in this listing

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LOF
Manufacturer City Province Registered as Device types
JKH Health Co., Ltd. Dongguan Guangdong Contract manufacturer 22

Record

Regulatory record for Xstim
Listed by Xstim Inc., United States
FDA product code LOF
Device type Stimulator, Bone Growth, Non-Invasive
Device class Class 2
Regulation 21 CFR 890.5870
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) P230025
Record published 2024-08-16

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date, serial number
Packaging Pack of 5

Catalogue Numbers

Catalogue numbers for Xstim
Catalogue number Size Status
07-5006 In distribution
08-1096 In distribution
07-5003 In distribution
07-5004 In distribution
07-5001 In distribution
08-0041 In distribution
07-5005 In distribution
07-5007 In distribution
03-5005 In distribution
07-5000 In distribution
07-5002 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pemf – Physio-Stim Orthofix US LLC 39
Physio-Stim Orthofix US LLC 26
Biomet EBI Bone Healing System EBI, LLC 24
Biomet SpinalPak / OrthoPak EBI, LLC 18
Orthofix Osteogenesis Stimulator Orthofix US LLC 16
ActaStim-S Theragen, Inc. 11
CMF DJO, LLC 8
Biomet SpinalPak Non-invasive Spine Fusion Stimulator System EBI, LLC 7
Cervical-Stim Orthofix US LLC 7
Biomet OrthoPak Non-invasive Bone Growth Stimulator System EBI, LLC 6
Accelstim Igea SPA 6
Spinal Stim Orthofix US LLC 6

Showing 12 of 21. All products under Stimulator, Bone Growth, Non-Invasive

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P210016 2025-01-17 ManaFuse Enovis
P230025 2024-11-12 Xstim Spine Fusion Stimulator Xstim Inc.
P790002 2022-11-23 Biomet® OrthoPak Non-invasive Bone Growth Stimulator System Ahp Eos Buyer, Inc.
P190030 2022-06-17 ActaStim-S Spine Fusion Stimulator Theragen, Inc.
P210035 2022-05-03 AccelStimTM Bone Growth Stimulator Orthofix US LLC
P850007 2018-08-22 PhysioStim, SpinalStim Orthofix SRL
P900009 2017-09-11 EXOGEN Ultrasound Bone Healing System Bioventus LLC
P850022 2015-09-09 BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATORY SYSTEM AND BIOMET ORTHOPAK NON-INVASIVE BONE GROWTH STIMULATOR Ahp Eos Buyer, Inc.
P030034 2009-09-11 CERVICAL-STIM Orthofix SRL
P910066 1997-01-03 ORTHOLOGIC (TM)1000 BONE GROWTH STIMULATOR DJO, LLC

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