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PrestiVac

Vacuum solutions engineered for medical device manufacturing

The floor where a combustible-metal machine shop and a cleanroom occupy the same room — implant-grade titanium, cobalt-chromium and nitinol are machined into devices that must then stay contamination-free for biocompatibility, so recovery has to satisfy two normally-separate disciplines at once: rated for reactive-metal fines, and clean enough for a controlled environment.

  • Two Disciplines, One Tool

    Metal-rated and cleanroom-clean

  • Reactive-Metal Aware

    Titanium, cobalt-chrome & nitinol

  • Contamination Control

    Biocompatibility is the spec

  • HEPA Filtration

    Fine and toxic fractions retained

  • Explosion-Proof

    Manufacturing specialists

  • 1000+

    Vacuums sold worldwide

  • USA

    Designed & manufactured

  • Direct

    Buy from the manufacturer

  • NFPA 660

    ATEX / IECEx principles

Medical Device Manufacturing production process explorer

Every stage. Every challenge. The right vacuum solution.

Device manufacturing runs from raw implant-grade stock to sterile, packaged product — combining precision machining with contamination control. Walk the stages where the two disciplines meet.

Stage 01Implant-metal machining

Titanium, cobalt-chromium and nitinol are machined into implants and instruments, shedding fine reactive-metal chips and dust that carry combustible-metal rules from the first cut.

Key challenges

A machine shop inside a cleanroom

  • Reactive-Metal Fines

    Machining titanium, cobalt-chromium and nitinol generates combustible metal dust — the reactive-metal rules apply on a floor most people picture as pristine.

  • Biocompatibility Is Contamination

    Device surfaces must stay contamination-free for biocompatibility, so housekeeping is a quality-and-safety control, not a cosmetic one.

  • Two Rules At Once

    Recovery must be combustible-metal-rated and cleanroom-clean simultaneously — a combination few generic vacuums satisfy.

  • Cobalt Exposure

    Cobalt-chromium alloys add a health dimension — cobalt fines carry occupational-exposure concern, demanding HEPA retention and sealed handling.

  • Polymer Dust Too

    PEEK, UHMWPE and other machined medical polymers shed combustible plastic dust with static behavior, alongside the metal fines.

  • Validated Cleanliness

    Cleanliness is documented against the device quality system, so recovery equipment must be qualified as part of a validated, auditable process.

Dust & materials knowledge center

What device manufacturing generates

Common Medical Device Manufacturing materials and recovery approaches
MaterialCombustibleRecovery approachDeep dive
Titanium finesYes — reactive metalGrounded, rated recovery; immersion where required
Cobalt-chromium dustCombustible + toxicHEPA-retained, sealed; cobalt exposure control
Nitinol & specialty alloysReactiveCombustible-metal discipline; test the fines
Medical polymers (PEEK, UHMWPE)Yes — and self-chargingGrounded, static-dissipative recovery
Stainless & instrument metalsGenerally lowerHEPA recovery; contamination control
Surface-treatment residuesVariesSealed recovery supporting biocompatibility

Combustibility and severity are material- and particle-size-specific — testing and your Dust Hazard Analysis govern. Full directory: the full materials directory.

Talk to the manufacturer

Get the right explosion proof vacuum for your application.

Tell us what you need to vacuum and where. Our technical team will recommend the PrestiVac model best suited to your material, your classification and how hard you will work it — and because we build every unit ourselves, we can modify it to fit.

  • Legally certified explosion proof
  • Solid stainless steel construction
  • Industry-best 3-year warranty
  • Designed & manufactured in the USA
  • 200+ vacuum versions