Intromedic Co., Ltd.
Intromedic Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2026, with 1 FDA device recall on record.
Top product codes for Intromedic Co., Ltd.
FDA recalls by Intromedic Co., Ltd.
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 Intromedic Co., Ltd.
- K252617 — MiroCam® Capsule Endoscope System
- K180732 — MiroCam Capsule Endoscope System
- K170438 — MiroCam Capsule Endoscope System
- K143663 — MiroCam Capsule Endoscope System
- K134005 — MIROCAM CAPSULE ENDOSCOPE SYSTEM
- K140751 — MIROCAM CAPSULE ENDOSCOPE SYSTEM
- K131131 — E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEM
- K123428 — MIROCAM CAPSULE ENDOSCOPE SYSTEM
- K120702 — E.G. SCAN II ESPHAGOSCOPE SYSTEM
- K111450 — MIROCAM CAPSULE ENDOSCOPE SYSTEM
- K111030 — E.G. SCAN (TM) ESOPHAGOSCOPE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.