# Biostim, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1980–1985): 5 510(k) clearances
- Product codes: GZJ (2), IPF (1), GXY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K844023: Aquaform Electrodes with Aquapore (Feb 1, 1985)
- K840725: Clinical Care Stimulator (Apr 18, 1984)
- K840724: Muscle Stimulator X-10 (Mar 5, 1984)
- K820678: System 10 (Mar 23, 1982)
- K802227: Anastim II Transcutaneous Electrical (Sep 26, 1980)

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