MARKETS
Full-service development and manufacturing across six markets
From early product design and DFM through tooling, molding, assembly, packaging, and logistics, Alentra brings every capability together with one partner, a single-source model that reduces handoffs and keeps your program moving, whatever your market.
MARKETS
Full-service development and manufacturing across six markets
From early product design and DFM through tooling, molding, assembly, packaging, and logistics, Alentra brings every capability together with one partner, a single-source model that reduces handoffs and keeps your program moving, whatever your market.
MARKETS WE SERVE
Six markets, one
accountable partner.
Each market has its own requirements. Alentra brings the engineering, manufacturing, and quality capabilities to support them all.
Medical Device
Class I–III medical devices and components supported by cleanroom manufacturing, assembly, and ISO 13485 quality systems.
Drug Delivery
Autoinjector pens, wearable delivery devices, injection systems, and therapeutic delivery platforms manufactured with the precision, repeatability, and scale these programs demand.
Diagnostic
Diagnostic cartridges, test kits, reagent labware, and single-use consumables, supported by integrated molding and assembly.
Pharmaceutical
Ophthalmic bottles, dropper tips, and precision closures for pharmaceutical primary packaging, supported by molding and assembly expertise.
Life Science
Pipettes, blood-testing components, media bottles, and bioprocess single-use systems and consumables.
Consumer & Packaging
Medicine bottles, personal care packaging, canisters, jars, closures, and trays, supported by custom blow molding and scalable production.
Have a program that spans markets or requires a specialized approach?
WHY Alentra
One partner for every market you serve.
Quality & Compliance
Documented quality.
Proven control.
An ISO 13485:2016-certified quality management system, FDA registration, SPC, specialized inspection, and validation support provide documented control throughout production.
Connected Capabilities
One accountable team
across the lifecycle
Design, tooling, molding, assembly, packaging, and logistics are coordinated through one accountable team—reducing handoffs and maintaining continuity from development through production.
Cleanroom Manufacturing
Class 7 and 8 capacity
where it matters
Seven Class 7 and 8 cleanrooms support controlled molding and assembly for medical, drug-delivery, diagnostic, and other regulated programs.
QUALITY & COMPLIANCE
Quality and Regulatory Planning from the Start.
Across every market, quality has to be more than a claim. Our ISO 13485 quality management system, FDA registration, validation services, and inspection capabilities provide documented support from development through production.
- ISO 13485:2016 quality management system
The core medical-device quality standard, applied across our operations. - FDA registered
Supporting regulated medical, pharmaceutical, and diagnostic production. - IQ / OQ / PQ validation services
Process validation and capability studies integrated into development. - Statistical process control & inspection
Full SPC, full-dimensional and in-line inspection, and weekly reporting on corrective actions.
Ready to take the next step?
Whether you're in early concept, tooling, validation, or scale-up, we'll bring together the expertise and capabilities your program needs for its next stage.
Locations
U.S. capacity,
coast to coast.
Anchored by our Auburn, NY operations, Alentra's coast-to-coast footprint supports product development, molding, cleanroom manufacturing, assembly, and logistics. With manufacturing facilities and warehouses spanning the East and West Coasts, we help strengthen supply continuity and keep programs production ready.
6
Manufacturing Facilities
7
ISO Class 7 & 8 Cleanrooms
167
Molding Machines
5
Coast-to-coast Warehouses
Ready to move your program forward?
Whatever your market or stage of development, Alentra brings together the expertise, quality systems, and manufacturing capabilities needed to move your program from concept through production.