RGN

RGN 21G x 150mm, with injection tube, facet grinding 18 degree,

Registry build 21.09.26
1manufacturer
3catalogue numbers in this listing
1510(k) clearance

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 GXI
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24

Record

Regulatory record for RGN
Listed by Pajunk Gmbh Medizintechnologie, Germany
FDA product code GXI
Device type Probe, Radiofrequency Lesion
Device class Class 2
Regulation 21 CFR 882.4725
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Private-label distributor, Complaint-file establishment, Manufacturer
510(k) K060397
Record published 2026-06-10
Record revised 2025-12-01 (version 2)

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment humidity 20 to 65 % RH; Storage environment temperature 10 to 30 °C
Packaging Pack of 10
Sizes Needle gauge 21 to 23 G; length 60 to 150 mm

Catalogue Numbers

Catalogue numbers for RGN
Catalogue number Size Status
001160-40 Needle Gauge 21.0 G In distribution
001160-10 Length 60.0 mm In distribution
001160-20 Length 100.0 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OWL Diros Technology, Inc. 345
Probe, Radiofrequency Lesion Boston Scientific Neuromodulation Corporation 175
Halyard Avanos Medical, Inc. 156
Lccs Lccs Products Limited 101
Epimed Epimed International, Inc. 100
Avanos Avanos Medical, Inc. 89
NeuroTherm™ Neurotherm, Inc. 87
Probe, Radiofrequency Lesion St. Jude Medical 66
cannulaRFK Cosman Medical, Inc. 56
Rftl Pajunk Gmbh Medizintechnologie 54
Radiofrequency (RF) Needle Spectra Medical Devices, LLC 49
cannulaCC Cosman Medical, Inc. 47

Showing 12 of 85. All products under Probe, Radiofrequency Lesion

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K060397 2006-08-31

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