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Data / Medical devices / Perimeter, Automatic, Ac-Powered / United States

FDA-registered makers of Perimeter, Automatic, Ac-Powered in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Perimeter, Automatic, Ac-Powered (product code HPT). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. 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 of this device in the United StatesWatch these makers
Device
Perimeter, Automatic, Ac-Powered
Product code
HPT
Country
United States

Makers of Perimeter, Automatic, Ac-Powered in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Carl Zeiss Meditec IncDublin, CA, United StatesManufacturer, Specification developer1November 24, 1995000api.fda.gov
Konan Medical Usa, Inc.Irvine, CA, United StatesComplaint file establishment, Manufacturer, Specification developer1August 2, 2007000api.fda.gov
Novavision, Inc.Boca Raton, FL, United StatesManufacturer1April 22, 2003000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesManufacturer0000api.fda.gov
Heru, Inc.Miami, FL, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
KYS Vision, Inc.Elko, NV, United StatesComplaint file establishment, Specification developer0000api.fda.gov
M&S TechnologiesNiles, IL, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
M&S TechnologiesThayne, WY, United StatesManufacturer0000api.fda.gov
Medneuroptek Inc.Johns Creek, GA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Micro Medical Devices, Inc.Calabasas, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Morgan Newton CompanyPlano, TX, United StatesContract manufacturer0000api.fda.gov
Nidek IncorporatedThe Colony, TX, United StatesManufacturer0000api.fda.gov
Olleyes, Inc.Summit, NJ, United StatesManufacturer0000api.fda.gov
Peripherex Inc.Menlo Park, CA, United StatesManufacturer0000api.fda.gov
Ray Vision Inc.Lake Forest, CA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
RadiusXR Inc.Pleasanton, CA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Sight Intelligence Engineering CorporationFairfax, VA, United StatesManufacturer0000api.fda.gov
VIRTUAL FIELD, IncBrooklyn, NY, United StatesManufacturer0000api.fda.gov
Virtual Vision HealthMiami, FL, United StatesManufacturer0000api.fda.gov
Vivid VisionSan Francisco, CA, United StatesSpecification developer0000api.fda.gov

Updated November 2, 2026. 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.