What is FDA product code HRX?

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Orthopedic › DiagnosticArthroscope

Disc-FX® Guidewire

Name: Disc-FX® Guidewire
Brand: Disc-FX® Guidewire

3 catalogue numbers from DFX-GW-S/1, listed by Elliquence LLC, United States, under Arthroscope. 21 manufacturers in China are registered for this product code.

Registry build 21.09.26

21manufacturers in China registered for this device type

3catalogue numbers in this listing

1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (7), Jiangsu (6), Guangdong (5). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRX
Manufacturer	City	Province	Registered as	Device types
Modern Medical Equipment Manufacturing Ltd.	Heng Li, Dongguan	Guangdong	Contract manufacturer	26
Dongguan BAO Kang Dian ZI KE JI Limited	Dongguan	Guangdong	Contract manufacturer	24
Sanmina	Kunshan	Jiangsu	Contract manufacturer	15
Peter’s Technology (Suzhou) Co., Ltd.	Suzhou	Jiangsu	Contract manufacturer	9
Jiangsu Shenli Medical Production Co., Ltd.	Changzhou	Jiangsu	Contract manufacturer	6
PAN-International Precision Electronic Co., Ltd.	Dongguan	Guangdong	Contract manufacturer	4
Zimmer (Shanghai) Medical International Trading Co., Ltd.	Shanghai	Shanghai	Exporter	106
Shanghai JPY ION-Tech Co., Ltd.	Shanghai	Shanghai	Contract manufacturer	70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd.	Changzhou	Jiangsu	Manufacturer	53
Hangzhou Fushan Medical Appliance Co., Ltd.	Hangzhou	Zhejiang	Contract manufacturer	44
Arthrex (Shanghai) Co., Ltd.	Shanghai	Shanghai	Exporter	38
Goals Sterilization Co., Ltd.	Jiaxing	Zhejiang	Contract manufacturer	26

Showing 12 of 21. All 21 manufacturers in China registered for Arthroscope

Record

Regulatory record for Disc-FX® Guidewire
Listed by	Elliquence LLC, United States
FDA product code	HRX
Device type	Arthroscope
Device class	Class 2
Regulation	21 CFR 888.1100
Establishment	Specification developer, Complaint-file establishment, Manufacturer
Record published	2018-07-26
Record revised	2024-12-23 (version 3)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Supplied sterile	Yes
Single use	Yes
Label carries	lot or batch number, expiry date
Packaging	Box (dfx-gw-s) of 10, box (dfx-gw-18) of 10, box (dfx-gw-20) of 10

Catalogue Numbers

Catalogue numbers for Disc-FX® Guidewire
Catalogue number	Size	Status
DFX-GW-S/1		In distribution
DFX-GW-18/1		In distribution
DFX-GW-20/1		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Surgical Direct	Surgical Direct, Inc.	299
Arthroscope	Karl Storz GmbH & Co. KG	278
Conmed/Linvatec	Provision	265
Arthroscope	Smith & Nephew, Inc.	255
Medline	Medline Industries, Inc.	205
Arthroscope	Sterilmed, Inc.	184
Sustainable Technologies	Provision	150
Medline Renewal	Medline Industries, Inc.	123
Stryker	Provision	113
Arthrex®	Arthrex, Inc.	109
Arthrex	Provision	109
Eberle	Eberle GmbH & Co. KG	92

Showing 12 of 567. All products under Arthroscope

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K180766	2018-06-11

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.