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Data / Medical devices / United Kingdom / Beaver-Visitec International, Ltd

Beaver-Visitec International, Ltd: FDA-registered device maker in BIDFORD-ON-AVON Warwickshire, United Kingdom, 1 510(k) clearance

Beaver-Visitec International, Ltd is registered with the FDA (registration 9680620) in BIDFORD-ON-AVON Warwickshire, United Kingdom. It lists 31 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 12, 1983. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this oneWatch Beaver-Visitec International, Ltd
FDA registration number
9680620
FEI number
3002808441
Address
Waterloo Industrial Estate, BIDFORD-ON-AVON Warwickshire, United Kingdom, B50 4JH
Owner or operator
Beaver-Visitec International, Inc. (10033379)
Roles
Manufacturer, Specification developer
First device listed
August 10, 2010
Registered through
2026
Brand names listed
45 Degree Toothed Forceps, 50 Cannula, Adson Forceps Non-Toothed, Adson Forceps Toothed, Alphonso Paediatric Speculum, Angled Tying Forceps (McPherson), Anterior Chamber Cannula, Anterior Chamber Cannula [Rycroft] and more

Devices it lists

DeviceProduct codeClassRoleSource
Caliper, OphthalmicHOE1Manufactureraccessdata.fda.gov
Cannula, OphthalmicHMX1Manufactureraccessdata.fda.gov
Clamp, Eyelid, OphthalmicHOD1Manufactureraccessdata.fda.gov
Clip, Iris RetractorHOC1Manufactureraccessdata.fda.gov
Corneal Inlay Inserter HandleQGJ1Manufactureraccessdata.fda.gov
Curette, OphthalmicHNZ1Manufactureraccessdata.fda.gov
CystotomeHNY1Manufactureraccessdata.fda.gov
Depressor, OrbitalHNX1Manufactureraccessdata.fda.gov
Device, Irrigation, Ocular SurgeryKYG1Manufactureraccessdata.fda.gov
Dilator, LachrymalHNW1Manufactureraccessdata.fda.gov
Forceps, OphthalmicHNR1Manufactureraccessdata.fda.gov
Guide, Needle, SurgicalGDF1Manufactureraccessdata.fda.gov
Handle, ScalpelGDZ1Manufactureraccessdata.fda.gov
Hook, OphthalmicHNQ1Manufactureraccessdata.fda.gov
Hook, Surgical, General & Plastic SurgeryGDG1Manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Manufactureraccessdata.fda.gov
Knife, OphthalmicHNN1Manufacturer, Specification developeraccessdata.fda.gov
Marker, OcularHMR1Manufactureraccessdata.fda.gov
Marker, ScleraHMQ1Manufactureraccessdata.fda.gov
Needle, Aspiration And Injection, DisposableGAA1Manufactureraccessdata.fda.gov
Needle, Ophthalmic SuturingHNM1Manufactureraccessdata.fda.gov
Probe, LachrymalHNL1Manufactureraccessdata.fda.gov
Punch, Corneo-ScleralHNJ1Manufactureraccessdata.fda.gov
Retractor, OphthalmicHNI1Manufactureraccessdata.fda.gov
Scissors, OphthalmicHNF1Manufactureraccessdata.fda.gov
Spatula, OphthalmicHND1Manufactureraccessdata.fda.gov
Specula, OphthalmicHNC1Manufactureraccessdata.fda.gov
Spoon, OphthalmicHNB1Manufactureraccessdata.fda.gov
Spud, OphthalmicHNA1Manufactureraccessdata.fda.gov
Surgical Eye TrayPZG1Manufactureraccessdata.fda.gov
Trephine, Manual, OphthalmicHRH1Manufactureraccessdata.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
July 12, 1983K831901LACIMAL INTUBATION SETSHNLSubstantially EquivalentVisitec Co.accessdata.fda.gov

Compare with other makers

Updated July 12, 1983. 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.