DNA ProductsMedical, Clinical & Laboratory ProductsEvidence & Crime Scene Investigative ProductsContract Manufacturing

Life Science and Forensic Products

Premier Front End Applications for Specimen Collection through Sample Processing

  • Front end collection, storage systems and sample processing for applications in Life Sciences(Biomolecular, Protein, DNA, Clinical, Medical, Diagnostic, etc), Laboratory, Forensic & Crime Scene/Evidentiary
  • Pioneer in the invention and/or commercialization of new genomic, lab and forensic technologies and products.As per DNA FITZCO® Cards, MultiBarrier Pouch (1991), The DNA Card (1991), "Classic" Card (1991) FTA®(1993), DRYPAK®(1994), Omni Swabs(1995), C.E.P.™ Swabs(1995) Sampact®(2003), SpinEze® Pushoff™ Swab(2003), SpinEze® Baskets (2004), FP705 DNA Paper(2005), Re-introduction of CEP™ Swab(2009), Ensemble™, PRO™, PROi™, 705™ & 705i™(2010), FITZCO® Indicating Cards, ProPRIME™, ProPRIMEi™, DRI™ Cards, BIO™ DBS/DSS Cards (2011), etc...
  • Dedicated to developing and supplying specimen collection, transport and storage products, packaging solutions and customized specimen collection.

  • The premier BioSample collection device manufacturer. Since 1991, Fitzco has developed and manufactured millions of DNA kits and products for use in the data basing, identification, forensic and medical fields.

  • Quality - Fitzco is the only Manufacturer of Forensic & DNA Collection kits and products that is ISO 9001:2008 Certified, cGMP Compliant, Class I and Class III Medical Device Facility, FDA Inspected, with a Clean Room of 10,000/100,000. Our quality standards are unparalleled.
  • At Fitzco we take great pride in offering high quality products, competitive prices. Our friendly, knowledgeable staff will help you develop a packaging system that is right for you.

 

705™ Specimen CardsLineEnsemble Collection System™ - ECS™LineFP705™ Specimen Grade PaperLineFTA® DNA CardsLinePRO™ Protein/DNA/RNA  CardsLineProPRIME™ Protein/DNA/RNA Cards

ISO 9001:2008 Certified - Clean Room 10,000/100,000 - cGMP Facility - FDA Approved Class I & III Medical Device Facility
4300 Shoreline Drive Spring Park Minnesota, USA 55384
952.224.2700 TF 800.367.8760 .............Fax 952.224.2717 Fax TF 877.471.1185............. Fitzco@FitzcoInc.com