Perouse Medical

POLYSITE ®Pressure injectable Implantable Infusion Port with silicone-filled suture holes

Registry build 21.09.26
2manufacturers in China registered for this device type
4catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (1), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LJT
Manufacturer City Province Registered as Device types
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Forefront Medical Technology (Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 14

Record

Regulatory record for Perouse Medical
Listed by Perouse Medical, France
FDA product code LJT
Device type Port & Catheter, Implanted, Subcutaneous, Intravascular
Device class Class 2
Regulation 21 CFR 880.5965
Establishment Specification developer, Manufacturer
510(k) K122834
Record published 2026-01-22

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

Catalogue Numbers

Catalogue numbers for Perouse Medical
Catalogue number Size Status
3015SPIMST In distribution
2015SPIMST In distribution
2015SPI In distribution
3015SPI In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Dignity® Medical Components Inc 168
Deltec ICU Medical, Inc 130
NorPort Vascular Access Port Norfolk Medical 106
BioFlo Vortex AngioDynamics, Inc. 60
BioFlo Vortex Navilyst Medical, Inc. 59
Dignity® MID-Sized CT Port Medical Components Inc 55
TidalPort Vascular Access Port Norfolk Medical 52
Pro-Fuse® Low Profile CT Port Medical Components Inc 45
Dignity® Low Profile CT Port Medical Components Inc 45
Dignity® Mini CT Port Medical Components Inc 44
Medcomp GEN III Power Injectable Portmedcomp GEN III Power Injectable Port Medical Components Inc 29
PRO-Fuse® Medical Components Inc 28

Showing 12 of 96. All products under Port & Catheter, Implanted, Subcutaneous, Intravascular

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K122834 2013-12-11

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.

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