Pro-Med Instruments Gmbh
4 FDA 510(k) clearances · Recalling firm
◉ Watch Pro-Med Instruments Gmbh
| Record | Firm | Date |
|---|---|---|
| DORO Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002) recall (Z-1860-2025) | Pro-Med Instruments Gmbh | 2025-05-28 |
| DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous cranioto recall (Z-2970-2018) | Pro-Med Instruments Gmbh | 2018-09-17 |
| DORO LUCENT Locking Transitional Member, REF 1101.031 Component of headrest system used in recall (Z-2971-2018) | Pro-Med Instruments Gmbh | 2018-09-17 |
| DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open an recall (Z-2972-2018) | Pro-Med Instruments Gmbh | 2018-09-17 |
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Every clearance here is in the API, with alerts when new ones post.