Iantrek Inc.
Iantrek Inc. appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0134-2026, Class II) was initiated on September 6, 2025.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0134-2026 | Class II | Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300. Product Description: The | September 6, 2025 |
| Z-0135-2026 | Class II | C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: | September 6, 2025 |