Aju Pharm Co., Ltd.
Aju Pharm Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2024, with 8 FDA device recalls on record.
Top product codes for Aju Pharm Co., Ltd.
FDA recalls by Aju Pharm Co., Ltd.
- Z-1171-2026 — Genesis Push-In Suture Anchor
- Z-1167-2026 — Fixone Biocomposite Anchor
- Z-1170-2026 — Genesis Knotless Anchor
- Z-1169-2026 — Genesis Dual Thread Screw-In Anchor
- Z-1172-2026 — AlternatiV+ Max Knotless Anchor
- Z-1166-2026 — Fixone Hybrid Anchor
- Z-1173-2026 — AlternatiV+ Screw-In Anchor
- Z-1168-2026 — Genesis Screw-In Anchor
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 Aju Pharm Co., Ltd.
- K233601 — Fixone Meniscal Repair
- K230892 — Fixone Biocomposite Anchor
- K222423 — Fixone All Suture Anchor
- K203523 — Fixone hybrid knotless anchor
- K193497 — Fixone Biocomposite Interference Screw
- K192709 — Fixone All Suture Anchor
- K192484 — Fixone Biocomposite Anchor
- K192032 — Fixone Biocomposite Small Anchor
- K171299 — Fixone Biocomposite Anchor
- K162070 — JOINIX CANNULAR SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.