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TETmedical

1 viewer · 30d

Total raised

$3.5M

+$3.5M this year

1 filing since 2026 · latest Equity filed

Cumulative raised
LAST ROUND
Equity · $3.5M
ROUNDS
1
INVESTORS
45
FOUNDED
2021
HQ
Fair Haven, NJ
SECTOR
Biotech
EMPLOYEES
N/A
30D VIEWERS
1

AI overview

Updated

TETmedical, Inc. (Tethered Enzyme Technologies) is a clinical-stage nanomedicine diagnostics company spun out of Cornell University research, with labs at the Cornell Business & Technology Park in Ithaca, NY and an administrative office in Fair Haven, NJ. Its platform is a patented 'TET nanobot' — thousands of enzymes tethered to a nanoparticle — that performs chemical operations orders of magnitude faster than conventional antibody assays. Its lead product, NSE-FAST, is a rapid blood test to aid diagnosis of acute ischemic stroke, and received FDA Breakthrough Device Designation in June 2026. The platform is backed by more than $6M of NIH-funded research plus $2.8M in government grants, and the company was co-founded by serial medtech entrepreneur David Fischell with Cornell scientists Alex Travis and Roy Cohen.

What sets it apart

Tethering thousands of enzymes to a single nanoparticle produces signal amplification far faster than antibody-based assays, which is what makes a rapid point-of-care blood test for acute stroke feasible where existing workflows miss roughly 17% of ischemic strokes (up to 42% of atypical presentations).

Funding history

1 round
Equity+2Jun 12, 2026 · $10K min
Form D
+$3.5M$3.5M total

Latest SEC filings

via EDGAR · CIK 0001980705
Form D · Jun 12, 2026NewView on EDGAR

Products

1 tracked

NSE-FAST

In vitro diagnostic test

A rapid blood test measuring neuron-specific enolase functional activity, designed to aid in the diagnosis of acute ischemic stroke, including the atypical presentations most often missed in emergency settings.

  • Built on the TET tethered-enzyme nanoparticle platform for rapid signal generation
  • Targets the ~17% of US acute ischemic strokes currently missed, and ~42% for atypical presentations such as dizziness
  • Granted FDA Breakthrough Device Designation in June 2026
  • Blood-based, positioned for rapid use in acute care settings