# Micromed S.P.A.

- Location (FDA's records): Mogliano Veneto, IT
- FDA decisions: 7 (1987–2021): 7 510(k) clearances
- Names in FDA's records: Micromed S.P.A. (4); Micromed, Inc. (2); Micromed (1)
- Product codes: GZJ (2), DPS (1), OLV (1), GWQ (1), GWE (1), GYC (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Blackrock Neuromed: 2 (https://510kreport.com/company/blackrock-neuromed)
- Excel Tech., Ltd.: 1 (https://510kreport.com/company/excel-tech)
- Astro-Med, Inc.: 1 (https://510kreport.com/company/astro-med)
- Braebon Medical Corp.: 1 (https://510kreport.com/company/braebon-medical)
- Lifelines, Ltd.: 1 (https://510kreport.com/company/lifelines)

## Firms that cite its devices most
- Neuralynx, Inc.: 1 (https://510kreport.com/company/neuralynx)
- Blackrock Neuromed: 1 (https://510kreport.com/company/blackrock-neuromed)

## Its most-cited devices
- K071782: Micromed Brain Spy Plus, Embia Titanium Devices (2008), cited by 2
- K180761: SD LTM STIM Cortical Stimulator (2018), cited by 1

## Recent decisions
- K211974: LED PHOTIC System (Sep 23, 2021)
- K180761: SD LTM STIM Cortical Stimulator (Jun 18, 2018)
- K171384: Micromed BRAIN QUICK system (Feb 1, 2018)
- K071782: Micromed Brain Spy Plus, Embia Titanium Devices (Jan 10, 2008)
- K914762: Micro Med Inc. QRS-Card (TM) Office Ecg Monitor (Dec 5, 1991)
- K882980: Rebuilder Bucket System (Apr 24, 1989)
- K874085: Rebuilder (TM) (Dec 11, 1987)

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