# Newmark, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (2009–2016): 3 510(k) clearances
- Product codes: NUH (3)
- Predicates its devices cite: 8 (3 its own); citations of its devices by later devices: 8 (3 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
- Newcare Products, LLC: 2 (https://510kreport.com/company/newcare-products)
- Prizm Medical, Inc.: 2 (https://510kreport.com/company/prizm-medical)
- Gemore Technology Co, Ltd.: 1 (https://510kreport.com/company/gemore-technology)

## Firms that cite its devices most
- Triowave Technologies: 2 (https://510kreport.com/company/triowave-technologies)
- Marchan Medical, LLC: 1 (https://510kreport.com/company/marchan-medical)
- Hollywog, LLC: 1 (https://510kreport.com/company/hollywog)
- Acumed Medical, Ltd.: 1 (https://510kreport.com/company/acumed-medical)

## Its most-cited devices
- K090042: Painmaster MCT Patch (2009), cited by 4
- K130114: Painmaster MCT Patch (2013), cited by 4

## Recent decisions
- K151995: Painmaster MCT Patch (Oct 5, 2016)
- K130114: Painmaster MCT Patch (Apr 16, 2013)
- K090042: Painmaster MCT Patch (May 6, 2009)

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