Pall Posidyne® NEO Filter

Small volume 0.2 micron Air Eliminating Intravenous Filter for 96 Hour Use with Needle-free Injection Site and ultra-microbore tubing

Registry build 21.09.26
1manufacturer
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Registered in Zhejiang.

Chinese manufacturers registered for FDA product code FPB
Manufacturer City Province Registered as Device types
Hangzhou Qiantang Longyue Biotechnology Co., Ltd. Hangzhou Zhejiang Manufacturer 7

Record

Regulatory record for Pall Posidyne® NEO Filter
Listed by Global Life Sciences Solutions USA LLC, United States
FDA product code FPB
Device type Filter, Infusion Line
Device class Class 2
Regulation 21 CFR 880.5440
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K850825
Record published 2016-06-01
Record revised 2026-05-12 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Case of 50
Sizes Pore size 0.2 µm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Pall Posidyne® NEO Filter
Catalogue number Size Status
NEO96NY Pore Size 0.2 µm In distribution
NEO96 Pore Size 0.2 µm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Medex ICU Medical, Inc 44
Vygon Vygon Corp. 22
Pall Posidyne® ELD Filter Global Life Sciences Solutions USA LLC 5
GRI-BAG Laboratorios Grifols SA 3
Hemo-Nate Utah Medical Products, Inc. 3
Filter, Infusion Line Baxter Healthcare Corporation 3
Interlink Baxter Healthcare Corporation 3
Hemo-TAP Utah Medical Products, Inc. 2
Pall Supor® AEF Filter Pall International Sàrl 2
Spectrum, Inc. Spectrum Medical Ltd 2
WalkMed® WalkMed Technologies, LLC 2
Medline Industries, Inc. Medline Industries, Inc. 2

Showing 12 of 21. All products under Filter, Infusion Line

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K261403 2026-08-31

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