Fluid control for analytical & life sciences
Precision fluidics for the instruments that matter.
Ultra-reliable valves, manifolds and qualified sub-assemblies, engineered, machined, assembled and tested in-house for the world's leading OEMs.
Pressure
1,300 bar
Ports
2 to 24
Lifetime
> 1M cycles
Fig. 01 · Rotary shear valveAFP-RV series
630
Employees worldwide
7
Manufacturing facilities
302k
Sq ft production space
7/8
ISO Class cleanrooms
01What we do
Two ways to put AFP inside your instrument.
Buy proven AFP products off the shelf, or extend your own engineering team with our vertically integrated manufacturing platform.
Products
Premium rotary valves, diaphragm valves, manifolds, fittings and accessories that let OEMs push instruments to higher sensitivity, accuracy and repeatability.
Contract Manufacturing
Seamless access to precision machining, clean assembly, in-house testing and supply-chain services, from custom components to qualified sub-assemblies.
02Product families
Engineered for analytically clean, leak-free flow.
Ports
2 to 24
Pressure
Up to 1,300 bar
Wetted
PEEK, ceramic, SS316
Lifetime
>1M cycles
Rotary shear valves engineered for analytically clean, low-dispersion switching in LC, genomics and clinical diagnostic systems, built for millions of actuations without leaks or carry-over.
Explore rotary valves03Prototype to production
One partner across the entire product lifecycle.
Not a transactional supplier, AFP secures long-term partnerships and invests in your roadmap.
04Vertically integrated
Capabilities that extract cost and time from production.
Swiss multi-process machining
One work center producing parts that traditionally need four or five machines, breakthroughs in cost and cycle time.
ISO Class 7 & 8 cleanrooms
Electro-mechanical clean assembly that eliminates contamination for analytically clean results.
Overmolding & injection molding
Medical-grade polymers molded and overmolded in-house for consumables and components.
In-house testing
Leak, flow, pressure and functional testing with every part's quality history recorded.
Packaging & sterilization
Single and sterile-barrier packaging, kitting and validated sterilization management.
Supply chain & logistics
Procurement, warehousing, consignment inventory and lot-tracked delivery to your line.
05Quality system
Every part carries its own quality history.
AFP's data collection and tracking methodologies continuously record each part's history to ensure it meets or exceeds OEM specification, across seven ISO 13485-certified, FDA-registered facilities.
Our quality approachISO 13485
Medical device quality management
FDA
Registered manufacturing facilities
ISO 7 / 8
Electro-mechanical cleanrooms
IQ/OQ/PQ
Validated process methodology
06Industries served
Trusted where precision is non-negotiable.
01
Analytical instruments
Chromatography and spectrometry OEMs.
02
Clinical diagnostics
IVD analyzers and point-of-care systems.
03
Genomics & life science tools
Sequencing and sample-prep platforms.
04
Oil, gas & petrochemical
Process gas chromatographs and analyzers.
05
Semiconductor
Ultra-high-purity gas handling.
06
Industrial gases
Air separation and purity monitoring.
07
Environmental monitoring
Emissions and air-quality analyzers.
08
Medical devices
Components and assemblies under ISO 13485.