Garner, NC (Greater Raleigh)  |  Fast turnaround  |  service@jetsons.us  |  (919) 803-7507
Medical Devices

Precision Cleaning
for Medical
Manufacturers

Aqueous precision cleaning for surgical implants, instruments, and medical device components, without harsh chemicals or abrasives. Aligned with ISO 13485 and ASTM F2847, with full documentation for regulatory compliance.

ISO 13485 ASTM F2847 ISO 11607 IEST-STD-CC1246E
Surgical implants and instruments
Implantable components and surgical instruments cleaned using aqueous methods safe for biocompatible materials

Clean Parts. Regulatory Confidence.

Medical device manufacturers and contract manufacturers require cleaning processes that remove machining fluids, particulates, and biological contamination without altering material properties, surface finish, or biocompatibility of delicate components.

Jetsons uses aqueous cleaning technology specifically suited to medical applications: no harsh solvents, no abrasive media, and no risk of residue incompatible with downstream sterilization or packaging processes.

  • Orthopedic and spinal implants
  • Surgical instruments and cutting tools
  • Dental implants and prosthetic components
  • Fluid-path device components
  • Interstage washing during manufacturing
  • Pre-packaging cleanliness verification

Aqueous Cleaning for Sensitive Materials

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Aqueous Cleaning

Water-based cleaning systems remove machining oils, cutting fluids, and particulates from implant and instrument surfaces without chemical attack on sensitive alloys including titanium, cobalt-chrome, and PEEK.

Biocompatible safe
🔈

Ultrasonic Cleaning

High-frequency ultrasonic cavitation dislodges sub-micron particles from complex geometries, blind holes, and porous surfaces common in orthopedic and dental implant designs.

Complex geometries
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Interstage Washing

Cleaning between manufacturing operations removes process residues before they become bonded to surfaces. Critical for maintaining surface integrity in multi-step fabrication.

Manufacturing support
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Clean Packaging

Cleaned components are packaged in certified-clean barrier materials compliant with ISO 11607, maintaining cleanliness from our facility to your customer or sterilization provider.

ISO 11607
Medical instruments after precision cleaning
Surgical instruments after aqueous precision cleaning and pre-packaging inspection

Standards We Work To

ISO 13485
Quality management systems for medical devices
ASTM F2847
Standard practice for reporting cleanliness of implants
ISO 11607
Packaging for terminally sterilized medical devices
IEST-STD-CC1246E
Production cleanliness level applications

Cleanliness Verification & Records

Medical device manufacturers require documented evidence of cleanliness for design validation, production qualification, and regulatory submission. Jetsons provides in-house analytical verification and delivers a certificate of cleanliness with every shipment.

Our verification methods include NVR gravimetric testing, automatic particle counting, and UV/white light visual inspection. All results are documented with lot traceability, test method reference, acceptance criteria, and pass/fail determination.

Medical device clean room

Helping Medical Manufacturers
Meet Cleanliness Requirements

From interstage washing to pre-packaging verification, aqueous cleaning aligned with your regulatory and customer requirements.