Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Blackrock Microsystems with 3 510(k) clearances and 2 device recalls. The most recent is a 510(k) clearance dated Feb 10, 2021: Digital NeuroPort Biopotential Signal Processing System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 10, 2021 | Digital NeuroPort Biopotential Signal Processing SystemK202174 · GWL | 510(k) clearances |
| Feb 14, 2020 | Blackrock NeuroCoG Subdural Cortical Electrodes (Strips and Grids)K191346 · GYC | 510(k) clearances |
| Aug 10, 2016 | Patient Cable. Part Numbers: 4460, 6735. Sterile within Chipboard Boxes within corrugated cartons. Product Usage: The Blackrock NeuroPoClass II · Blackrock Microsystems, LLC announces a voluntary field action for the Blackrock NeuroPort Biopotential Signal Processin | Device recalls |
| Aug 10, 2016 | Neural Signal Amplifier. Part Numbers: 4208, 5703, 5749, 5748, 5747. Product Usage: The Blackrock NeuroPort Biopotential Signal ProcessiClass II · Blackrock Microsystems, LLC announces a voluntary field action for the Blackrock NeuroPort Biopotential Signal Processin | Device recalls |
| Feb 9, 2011 | NEUROPORT CORTICAL MICROELECTRODE ARRAY SYSTEMK110010 · GZL | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
