Universal Plastic Mold (UPM) serves OEMs in four industries from its 130,000 sq ft Baldwin Park, California facility: automotive aftermarket and specialty vehicles, industrial and high-end electronics, complex and reusable packaging, and non-sterile medical and laboratory equipment. UPM operates 30 injection molding machines from 150 to 2,000 tons, is ISO 9001:2015 certified and IATF 16949 compliant, and has been in continuous operation since 1962.

Use the table below to identify the UPM industry page that matches your program. Each industry name links to a dedicated sub-page with full capability detail, materials, certifications, and FAQs.

UPM supports automotive aftermarket and specialty vehicle OEMs — RV, upfit, service body, and accessory programs. Typical parts include truck caps, service-body panels, RV exterior components, step pads, interior consoles, mobile video and electronics housings, and structural mounting brackets.
UPM’s three 2,000-ton presses, ~540 oz shot capacity, and 94.5″ × 77.3″ platen enable large structural parts to be molded in one piece, in one facility. ISO 9001:2015 certified and IATF 16949 compliant; PPAP Level 3, First Article Inspections (FAI), APQP, and full lot-level traceability standard.
UPM does not currently serve Tier-1 passenger-car OEMs.
UPM molds enclosures, housings, and structural components for industrial controls, NEMA-rated equipment, EV chargers and kiosks, professional AV equipment, networking and IT infrastructure, test and measurement instruments, rugged handhelds, and protective cases.
UPM runs UL-listed flame-retardant grades for regulated applications, and integrates customer-supplied PCBs — functional and continuity testing, then installation into molded components — under one ISO 9001:2015 quality system.
UPM does not manufacture or populate PCB boards.


UPM is a long-standing molder for reusable and industrial packaging OEMs — pallets, totes, crates, bulk containers, and transport-grade dunnage. Primary materials are polypropylene (PP) and high-density polyethylene (HDPE), with glass-filled grades for load-bearing structural applications. UPM supports regrind and recycled-content resin blends where program specifications allow.
Programs typically run 5 to 10 years at hundreds of thousands to millions of pieces annually. Tooling stays in Baldwin Park, California under U.S. legal jurisdiction with full customer ownership and IP protection under U.S. law.
UPM molds housings and enclosures for non-sterile medical devices and lab equipment — benchtop diagnostic instruments, in-vitro diagnostic (IVD) instruments, lab automation, durable medical equipment (DME), and non-patient-contact components of Class I and Class II devices.
UPM does not produce sterile devices, sterile fluid-path components, or Class III implantables, and does not operate an ISO 13485 cleanroom. Programs requiring ISO 13485 / cleanroom manufacturing are best directed to specialist sterile-device molders.
UPM supports niche-medical economic minimums as low as 100 pieces per release — below the 500-piece minimum on other programs — reflecting typical diagnostic instrument and benchtop equipment volumes.

Across all four industries, UPM delivers:
30 injection molding machines from 150 to 2,000 tons at a 130,000 sq ft facility in Baldwin Park, California
ISO 9001:2015 certified (Certificate #1715, ISA); IATF 16949 compliant
PPAP Level 3, First Article Inspections (FAI), and full lot-level traceability standard
2–3 week post-tooling production lead times
Tooling held in the U.S. under U.S. legal jurisdiction, with full customer ownership and IP protection under U.S. law
One Account Manager who is also the Program Manager from quote through production
24-hour email reply standard; live phone answer during business hours
Family-owned and operating continuously since 1962; ~300 employees, $30M+ annual revenue
UPM serves automotive aftermarket and specialty vehicle OEMs, industrial and high-end electronics OEMs, complex and reusable packaging OEMs, and non-sterile medical and laboratory equipment OEMs.
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No. UPM produces non-sterile medical device and lab equipment components only. UPM does not operate an ISO 13485-certified cleanroom and does not produce sterile fluid-path components, sterile single-use devices, or Class III implantables.
UPM’s automotive practice is focused on aftermarket and specialty vehicle programs — RV, upfit, service body, accessory, emergency-vehicle, and specialty-vehicle programs. UPM does not currently serve Tier-1 passenger-car OEMs.
UPM is built for hard-tooled production programs with minimum economic runs of 500 pieces through annual volumes in the millions. Niche-medical and lab equipment programs run as low as 100 pieces per release, reflecting typical diagnostic instrument and benchtop equipment volumes.
All molding, finishing, assembly, and PCB integration occur at UPM’s 130,000 sq ft facility in Baldwin Park, California. Tooling remains in Baldwin Park under U.S. legal jurisdiction, with full customer ownership and IP protection under U.S. law.
UPM is ISO 9001:2015 certified (Certificate #1715, issued by Amtivo) and IATF 16949 compliant. PPAPs (Level 3), First Article Inspections (FAI), and full lot-level traceability are available as standard.
Typical UPM production lead times are 2 to 3 weeks post-tooling. Lead times for PPAP- and FAI-supported launches are quoted on a per-program basis.
Domestic injection molding across four industries — one accountable partner.
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