Devices

Device Recall Beaver Visitec International, Inc

Model / Serial
Lot Numbers: 3039720 3046211 3047770 3049473 3070763 3082330 3089827 3093682 3095941 3106407 3117874
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including KY, GA, MI, and NJ.
Product Description
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove || Part Number: 584649 || Ophthalmic surgical kits
Manufacturer
Beaver-Visitec International Inc.
1 Event
- Recall of Device Recall Beaver Visitec International, Inc

Manufacturer

Beaver-Visitec International Inc.

Manufacturer Address
Beaver-Visitec International Inc., 411 Waverley Oaks Rd Ste 229, Waltham MA 02452-8422
Manufacturer Parent Company (2017)
Tpg Capital Management L.P.
Source
USFDA

2 devices with a similar name

Learn more about the data here

Device Recall Beaver Visitec International, Inc.

Model / Serial
Lot Numbers: 3035614 3046205 3052693 3055885 3063181 3068806 3073917 3082315
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including KY, GA, MI, and NJ.
Product Description
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove || Part Number: 584569 || Ophthalmic surgical kits
Manufacturer
Beaver-Visitec International Inc.

Device Recall Beaver Visitec International, Inc

Model / Serial
Lot Numbers: 3038787 3046210 3061080 3078492 3093681 3095940 3108668
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including KY, GA, MI, and NJ.
Product Description
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove || Part Number: 584648 || Ophthalmic surgical kits
Manufacturer
Beaver-Visitec International Inc.

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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