Engineered for Your Environment
From semiconductor fabs to pharmaceutical cleanrooms, Abgenics products meet the exacting standards of the world's most demanding industries across America, Europe, Mexico, and Southeast Asia.
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Semiconductor & Electronics
Ultra-clean wipers and contamination control mats for wafer fabs, display manufacturing, and advanced electronics assembly where sub-micron particle control is mission-critical.
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Pharmaceutical & Life Sciences
Cleanroom wipers and contamination control products for GMP environments, aseptic fill lines, cell therapy suites, and medical device manufacturing worldwide.
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Critical Manufacturing & Research
Specialty textiles and polyethylene products for aerospace, nanofabrication, and R&D facilities — manufactured in our Class 10 and 100 cleanrooms.
Explore solutions →What contamination costs in each one, and what we send in against it
A fab, a fill suite and an aerospace clean bay do not work to the same particle limits, and they are not audited against the same documents. The product is specified to the class and the protocol you actually run, not to a generic "cleanroom" label.
Semiconductor and electronics
On a wafer, a single sub-micron particle in the wrong place is a dead die, and a static discharge too small to feel does the same job. Yield is the whole economics of a fab, so anything that touches a wafer, a tool or a reticle has to be predictable lot after lot.
Abgenics supplies knitted wipers for wafer and tool wipe-down, contamination control mats at fab and sub-fab entries, ESD control products for handling and assembly, and polyethylene bags for wafer, component and display packaging. Because the yarn and the film are made in house, a new wiper lot does not become an uncontrolled variable in your yield data.
Typical lines in a fab
- Cleanroom wipers, low-particle knit
- Contamination control mats at every entry
- ESD control products
- Cleanroom bags and polyethylene film for packaging
- IPA and mop systems for tool areas
Pharmaceutical and life sciences
GMP environments, aseptic fill lines, cell therapy suites and medical device assembly are governed by documentation as much as by air quality. What a wipe leaves behind matters as much as what it picks up, and an auditor will ask for the data behind both.
Wipers here are specified on residue: non-volatile residue and specific ionic content by short-term extraction to IEST RP CC-004.2, liquid particle counts to IEST RP CC-003.2, and FTIR identification, with conformance documentation available for the quality file. Contamination control mats hold the line at gowning rooms and airlocks, cleanroom bags carry components between zones, and mop systems and IPA solutions support the cleaning routines your procedures already define.
What the quality file gets
- Test methods named by standard and section
- Conformance documentation per product
- ISO 9001:2015 certified quality system behind every lot
- EU/CE certification, RoHS testing
- Traceability back to raw material
Critical manufacturing and research
Aerospace clean bays, nanofabrication and R&D facilities rarely fit a catalog. The environment is unusual, the part is unusual, or the protocol was written for one program. This is where a vertical manufacturer earns its keep: the textile is engineered to the application rather than picked from a shelf, and the polyethylene packaging is sized to the part rather than the nearest stock bag.
Specialty textiles for third-party organizations are a core Abgenics line, manufactured in Class 10 and Class 100 cleanrooms. Bring the specification and the environment it goes into, and the product is built to it.
How to specify a custom product
- The class of the environment it goes into
- The application: what it touches, what it must not leave behind
- Size, construction and edge treatment
- Packaging, labeling and cleanliness class at pack
- The quantity you expect to run