Cleanroom molding & assembly Medical / Healthcare
Cleanroom molding & assembly, controlled from press to assembly
ISO Class 8 cleanroom connects robotic all-electric molding with protected assembly and program coordination.
Controlled by designFour linked disciplines
Cleanroom manufacturing protects the environment around every critical handoff
Controlled air
Filtered circulation, environmental monitoring, and a full cleanroom air exchange every 50 seconds.
Controlled motion
All-electric molding and robotic handling support repeatable production with fewer uncontrolled touchpoints.
Controlled handling
Airlocks, gowning protocols, protected handling, and assembly support medical component production.
Controlled evidence
Material verification, particle-count monitoring, validation, inspection, and traceability support release decisions.
Environmental architectureContamination control
ISO Class 8 cleanroom production controls air, access, and activity
The medical facility uses filtered conditioned air, controlled entry, full gowning, and on-site particle-count monitoring to maintain a disciplined production environment around sensitive components.
The complete cleanroom air volume is exchanged every 50 seconds.
Interlocked doors help prevent outside air from moving directly into protected areas.
Hair covering, masks, gowns, gloves, and shoe covers are required before entry.
Protected production pathLive workflow
Cleanroom production stays controlled through four connected stages
Material identity, process conditions, protected handling, and release evidence remain connected through every sequential handoff.
Incoming material control
Verify resin identity before the cleanroom molding process begins
Incoming inspection includes FTIR scanning on every resin lot to confirm material integrity before resin becomes a production variable.
Explore material and dimensional inspectionCleanroom press platformPrecision-sized capacity
All-electric cleanroom molding delivers repeatable control from 55 to 110 tons
Four robot-equipped presses support precision medical components in the cleanroom environment, including a machine configured for demanding high-temperature materials.
Review engineering resin expertiseCleanroom capacity
- Presses
- 4 all-electric
- Clamping range
- 55–110 tons
- Handling
- Robot-equipped
- Material capability
- High-temperature option
Beyond the molding cycleProtected downstream work
Cleanroom assembly keeps sensitive components inside a coordinated production path
Infinity supports cleanroom molding, assembly, and pad printing within its dedicated medical facility.
Explore assembly capabilitiesQuality evidenceISO 13485 framework
Cleanroom quality depends on traceable material, process, and inspection evidence
Environmental discipline is one layer of the system. Material identity, process evidence, dimensional inspection, and documented release complete the picture.
Material integrity
Incoming FTIR scanning on every resin lot supports positive material identification.
Environmental monitoring
On-site particle-count monitoring provides evidence that the controlled environment remains on track.
Scientific process validation
Defined process windows help preserve repeatability from qualification into sustained production.
Inspection and traceability
CMM and vision-system capabilities connect dimensional results to documented program control.
One Southwest Indiana campusConnected expertise
Cleanroom production stays connected to a full technical campus
Infinity's Medical / Healthcare and Automotive / Industrial facilities share one campus, keeping specialized production close to the teams that solve tooling, automation, validation, and measurement challenges.
Specialized environments supported by one connected technical team.
Plan the protected pathStart with the program
Bring your next medical component to a controlled domestic manufacturing partner
Share the part, material, cleanliness expectations, assembly needs, and validation scope. Infinity's team can help define the right production path.