Iantrek Inc.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300. Product Descripti recall (Z-0134-2026) | Iantrek Inc. | 2025-10-10 |
| C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Descrip recall (Z-0135-2026) | Iantrek Inc. | 2025-10-10 |
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Every clearance here is in the API, with alerts when new ones post.