# Minrad, Inc.

- Location (FDA's records): Orchard Park, NY
- FDA decisions: 14 (1997–2007): 14 510(k) clearances
- Product codes: KNW (3), CCW (3), FMF (3), JAA (2), MDM (1), CBN (1), KKX (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 6 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Wilson Greatbatch Technologies, Inc.: 1 (https://510kreport.com/company/wilson-greatbatch-technologies)
- Fraser Harlake, Inc.: 1 (https://510kreport.com/company/fraser-harlake)

## Firms that cite its devices most
- Injectimed, Inc.: 1 (https://510kreport.com/company/injectimed)
- Rhythmlink International, LLC: 1 (https://510kreport.com/company/rhythmlink-international)
- Novamed, LLC: 1 (https://510kreport.com/company/novamed)
- Truphatek International, Ltd.: 1 (https://510kreport.com/company/truphatek-international)

## Its most-cited devices
- K041852: MR Tested Fiber Optic Short Laryngoscope Handle, Model 310002 (2004), cited by 3
- K013040: Light Saber Introducer Needle (2001), cited by 2
- K982735: Light Saber Bone Biopsy Needle (1998), cited by 1

## Recent decisions
- K072255: Minrad Inc. Nasal Scavenging Circuit (Oct 18, 2007)
- K071814: Light Sabre Spinal Access Device (Oct 16, 2007)
- K062231: MR Fiber Optic Intubating Laryngoscope Handle, Standard, Model 310001 (Aug 31, 2006)
- K062230: MR Fiber Optic Intubating Laryngoscope Handle, Short, Model 310002 (Aug 31, 2006)
- K041852: MR Tested Fiber Optic Short Laryngoscope Handle, Model 310002 (Nov 15, 2004)
- K041846: Sabresource Drape (Aug 26, 2004)
- K021084: Light Saber Spinal Needle (Jul 3, 2002)
- K013040: Light Saber Introducer Needle (Dec 7, 2001)

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