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Data / Medical devices / Mexico / Beaver-Visitec International, Inc.

Beaver-Visitec International, Inc.: FDA-registered device maker in Ciudad Juarez Chihuahua, Mexico, 6 510(k) clearances

Beaver-Visitec International, Inc. is registered with the FDA (registration 3013421458) in Ciudad Juarez Chihuahua, Mexico. It lists 36 device types. The FDA files 6 510(k) clearances under its listings, the newest dated April 17, 2017. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Beaver-Visitec International, Inc.
FDA registration number
3013421458
Address
Valle del Cedro No. 1520, Parque Industrial Intermex, Ciudad Juarez Chihuahua, Mexico, CP 32575
Owner or operator
Beaver-Visitec International, Inc. (10033379)
Roles
Contract manufacturer, Repackager or relabeler
First device listed
August 10, 2010
Registered through
2026
Brand names listed
45 Degree Toothed Forceps, 50 Cannula, Accu-Temp High Temperature Cautery, Accu-Temp High Temperature Cautery Handle, Accu-Temp Interchangeable Fine Tip, Accu-Temp Interchangeable Loop Tip, Accu-Temp Low Temperature Cautery, Accu-Temp Low Temperature Cautery Handle and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Repackager or relabeleraccessdata.fda.gov
Apparatus, ElectrosurgicalHAM2Contract manufactureraccessdata.fda.gov
Blade, ScalpelGES1Contract manufactureraccessdata.fda.gov
Cannula, OphthalmicHMX1Contract manufactureraccessdata.fda.gov
Clip, Iris RetractorHOC1Contract manufactureraccessdata.fda.gov
CystotomeHNY1Contract manufactureraccessdata.fda.gov
Device, Irrigation, Ocular SurgeryKYG1Contract manufactureraccessdata.fda.gov
Drape, Surgical, AntimicrobialKKX2Repackager or relabeleraccessdata.fda.gov
Electrosurgical, Cutting & Coagulation & AccessoriesGEI2Contract manufactureraccessdata.fda.gov
Forceps, OphthalmicHNR1Contract manufactureraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Repackager or relabeleraccessdata.fda.gov
General Surgery TrayLRO2Contract manufactureraccessdata.fda.gov
Gown, SurgicalFYA2Repackager or relabeleraccessdata.fda.gov
Handle, ScalpelGDZ1Contract manufactureraccessdata.fda.gov
Hook, OphthalmicHNQ1Contract manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Contract manufactureraccessdata.fda.gov
Kit, Surgical Instrument, DisposableKDD1Contract manufactureraccessdata.fda.gov
Knife, EarJYO1Contract manufactureraccessdata.fda.gov
Knife, EntKTG1Contract manufactureraccessdata.fda.gov
Knife, MyringotomyJYP1Contract manufactureraccessdata.fda.gov
Knife, OphthalmicHNN1Contract manufactureraccessdata.fda.gov
Knife, OrthopedicHTS1Contract manufactureraccessdata.fda.gov
Light, Examination, Medical, Battery PoweredKYT1Contract manufactureraccessdata.fda.gov
Marker, OcularHMR1Contract manufactureraccessdata.fda.gov
Needle, Aspiration And Injection, DisposableGAA1Contract manufactureraccessdata.fda.gov
Plug, PunctumLZUUContract manufacturer, Repackager or relabeleraccessdata.fda.gov
Probe, LachrymalHNL1Contract manufactureraccessdata.fda.gov
Ring CutterFNS1Contract manufactureraccessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)HOY1Contract manufactureraccessdata.fda.gov
Spatula, OphthalmicHND1Contract manufactureraccessdata.fda.gov
Specula, OphthalmicHNC1Contract manufactureraccessdata.fda.gov
Sponge, OphthalmicHOZ2Repackager or relabeleraccessdata.fda.gov
Surgical Eye TrayPZG1Repackager or relabeleraccessdata.fda.gov
Syringe, PistonFMF2Contract manufactureraccessdata.fda.gov
Trephine, Manual, OphthalmicHRH1Contract manufactureraccessdata.fda.gov
Unit, Cautery, Thermal, Battery-PoweredHQP2Contract manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 17, 2017K162361Soft Plug Extended Duration 180 Canalicular PlugLZUSubstantially EquivalentOasis Medical, Inc.accessdata.fda.gov
August 2, 2011K111067JIE+HONG MEDICAL SURGICAL GOWNS - STERILE, JIE+HONG MEDICAL SURGICAL GOWNS - NON STERILEFYASubstantially EquivalentKunshan Jiehong Nonwoven Product Co., Ltd.accessdata.fda.gov
June 27, 2002K013613SOFT PLUG ABSORBABLE PLUG-SALZUSubstantially EquivalentOasis Medical, Inc.accessdata.fda.gov
March 12, 2001K010572BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPEKKXSubstantially EquivalentBecton, Dickinson and Co.accessdata.fda.gov
February 7, 1995K946357COLLAGEN INTRACANALICULAR PLUGLZUSubstantially EquivalentOasis Medical, Inc.accessdata.fda.gov
May 18, 1990K900786VISI-SORB ABSORBANT STICKHOZSubstantially EquivalentVisitec Co.accessdata.fda.gov

Compare with other makers

Updated April 17, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.