FDA applicant
Bodyvision Medical, Ltd.
FDA records 4 decisions for Bodyvision Medical, Ltd. (Ramat Hasharon, IL) from 2017 to 2024: 4 510(k) clearances. Most are in product codes LLZ (System, Image Processing, Radiological) and EOQ (Bronchoscope (Flexible Or Rigid)). Since 2016 its 510(k)s took a median of 160 days from receipt to decision, against 124 for FDA’s reviews in the same codes and years. Its devices cite 3 predicates, 1 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Bodyvision Medical, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
Planning a device like Bodyvision Medical, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report