Instrumentation Laboratory (IL) Co.
Instrumentation Laboratory (IL) Co. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 20, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K260551 | HemosIL Factor V Leiden (APC Resistance V) | March 20, 2026 |
| K253957 | HemosIL Silica Clotting Time | January 9, 2026 |
| K251968 | HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL | July 24, 2025 |
| K243374 | HemosIL CL HIT-IgG(PF4-H) | January 28, 2025 |
| K242127 | ACL TOP Family 50 Series (ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LAS; ACL TOP 550 CTS; ACL TOP 35 | August 16, 2024 |