Beaver-Visitec International, Inc.
Beaver-Visitec International, Inc. holds FDA 510(k) medical device clearance, cleared in 2025, with 194 FDA device recalls on record.
Top product codes for Beaver-Visitec International, Inc.
FDA recalls by Beaver-Visitec International, Inc.
10 most recent of 194- Z-1008-2026 — BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
- Z-2800-2024 — BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000192;
- Z-2927-2024 — BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001943;
- Z-2842-2024 — BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001073;
- Z-2802-2024 — BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000266;
- Z-2845-2024 — BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001118;
- Z-2875-2024 — BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001486;
- Z-2853-2024 — BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001212;
- Z-2860-2024 — BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001338;
- Z-2880-2024 — BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001526;
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 Beaver-Visitec International, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.