# Millipore Corp.

- Location (FDA's records): Milford, MA
- FDA decisions: 33 (1977–2010): 32 510(k) clearances and 1 original PMA approval
- Names in FDA's records: Millipore Corp. (31); Millipore Corporation (2)
- Product codes: LDM (7), BSN (3), JRL (3), KIE (3), FIP (2), FPB (2), FIB (1), LKN (1), KPP (1), JJH (1), DPM (1), GLZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Aksys, Ltd.: 1 (https://510kreport.com/company/aksys)
- Merck Millipore, Ltd.: 1 (https://510kreport.com/company/merck-millipore)

## Its most-cited devices
- K934069: Millex, Dualex (Plus, Ultra) (1994), cited by 1
- K023892: Millex VV, GV, and HV Syringe Filter Units (2003), cited by 1

## Recent decisions
- K093815: Light Diagnostics Human Metapneumovirus Dfa Kit, Model Catalog Number 3124 (Mar 12, 2010)
- K081527: Light Diagnostics HSV 1/2 Typing Dfa Kit (Apr 1, 2009)
- K023892: Millex VV, GV, and HV Syringe Filter Units (Jan 17, 2003)
- K013988: Millex GP Sterilizing Filter Unit, Model SLGP 033 R (Apr 4, 2002)
- K963717: Millex - MP Filter Unit (SLMPO25SS/SLMPL25SS) (Jun 10, 1997)
- K941326: Ultrafree-CL (May 27, 1994)
- K934069: Millex, Dualex (Plus, Ultra) (Apr 21, 1994)
- K924347: Waters (TM) 996 Pda (Dec 11, 1992)

Source page: https://510kreport.com/company/millipore