Aizu Olympus Co., Ltd.
Aizu Olympus Co., Ltd. holds FDA 510(k) medical device clearance, cleared in 2005, with 31 FDA device recalls on record.
Top product codes for Aizu Olympus Co., Ltd.
FDA recalls by Aizu Olympus Co., Ltd.
10 most recent of 31- Z-0872-2026 — Olympus OER-Elite
- Z-0873-2026 — Olympus OER-Pro
- Z-0874-2026 — Olympus OER-Mini
- Z-0419-2024 — PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE
- Z-0417-2024 — GIF-HQ190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
- Z-0415-2024 — CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE
- Z-0418-2024 — PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE
- Z-0416-2024 — GIF-H190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
- Z-0346-2024 — Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery Model Numbers: TJF-145, TJF-150, TJF-Q180V, TJF-Q190V.
- Z-0348-2024 — Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the ureter and kidney. Model Numbers: URF-P7, URF-P7R, URF-V2, URF-V2R, URF-V3, URF-V3R.
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 Aizu Olympus Co., Ltd.
Data sourced from openFDA. This site is unofficial and independent of the FDA.