VitreQ BV
VitreQ BV holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2020, with 16 FDA device recalls on record.
Top product codes for VitreQ BV
FDA recalls by VitreQ BV
10 most recent of 16- Z-0859-2020 — VitreQ 23G Blunt Needles with luer-lock connector-REF: CN23.D05 GTIN: 8719214221621
- Z-0854-2020 — VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485
- Z-0852-2020 — VitreQ 25G VFI Cannula-REF: CN25.D03 GTIN: 8719214221447
- Z-0853-2020 — VitreQ 27G VFI Cannula-REF: CN27.D03 GTIN: 8719214221461
- Z-0857-2020 — VitreQ 23G Pick Needles-REF: CN23.D04 GTIN: 8719214221584
- Z-0849-2020 — VitreQ 23G PFC Injection Needle- Ref: MD23.D01 GTIN: 8719214221362
- Z-0856-2020 — VitreQ 25G Silicone Tipped Cannula-REF: CN25.D01 GTIN: 8719214221522
- Z-0847-2020 — (1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G BF Brush Needles-BF25.D52 GTIN: 8719214221188
- Z-0858-2020 — VitreQ 25G Pick Needles-REF: CN25.D04 GTIN: 8719214221607
- Z-0846-2020 — (1) VitreQ 23G BF Blunt Needles-BF23.D51 GTIN#: 8719214221126 (2) VitreQ 23G BF Brush Needles-BF23.D52 GTIN#: 8719214221140
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 VitreQ BV
Data sourced from openFDA. This site is unofficial and independent of the FDA.