Centerline Biomedical, Inc.
Centerline Biomedical, Inc. holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2026, with 1 FDA device recall on record.
Top product codes for Centerline Biomedical, Inc.
FDA recalls by Centerline Biomedical, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Centerline Biomedical, Inc.
- K254089 — IOPS Visionary System (MC-3) +7 more
- K243842 — Intra-Operative Positioning System (IOPS®)
- K242133 — Intra-Operative Positioning System (IOPS®) (Fiducial Tracking Pad) +1 more
- K241243 — Intra-Operative Positioning System (IOPS®) Viewpoint (Simple Curve Catheters) +1 more
- K230309 — Intra-Operative Positioning System (IOPS®) (MC-1) +4 more
- K190106 — Intra-Operative Positioning System +4 more
Data sourced from openFDA. This site is unofficial and independent of the FDA.