Taewoong Medical Co., Ltd.
Taewoong Medical Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2026, with 1 FDA device recall on record.
Top product codes for Taewoong Medical Co., Ltd.
FDA recalls by Taewoong Medical 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 Taewoong Medical Co., Ltd.
- K260962 — Sphincterotome
- K252648 — Niti-S SPAXUS Stent
- K251123 — Niti-S Biliary Stent; Niti-S Biliary Slim M Stent
- K243619 — Niti-S Esophageal Stent; Esophageal TTS Stent
- K250663 — Niti-S Duodenal Comfort Stent, Niti-S Colonic Comfort Stent
- K223067 — Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent
- K223626 — Niti-S Biliary Speed D Stent
- K223256 — Optimos Cystotome
- K221482 — Esophageal TTS Stent
- K221071 — Niti-S Biliary Slim M Stent
- K211706 — Esophageal TTS Stent
- K123205 — ESOPHAGEAL TTS STENT
- K113551 — ESOPHAGEAL TTS STENT
- K080782 — NITI-S ESOPHAGEAL STENT
- K073667 — NITI-S BILIARY STENT
- K041648 — NITI-S STENT & INTRODUCER, MODEL EOXXXX
Data sourced from openFDA. This site is unofficial and independent of the FDA.