Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1226011

FEI Number

3002532015

Entity Name

MICROVISION, INC.

City/State/Country

SEABROOK, NH, US

Establishment Address

20 London Ln, SEABROOK, NH 03874, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MicroVision, Inc. (Owner Number: 9034466)

Owner / Operator Contact Address

20 London Lane, Seabrook, NH 03874, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K982462

PMA Number

N/A

All Registered Proprietary Names

Fiber Optic Endoillumination Probe

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FFS	Image, Illumination, Fiberoptic, For Endoscope	Gastroenterology, Urology	Class 2	876.1500	2013-03-14

Official Correspondent

Danielle Clement

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MicroVision, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1226011. Last updated year: 2026. Please use registration number 1226011 when referencing this establishment in official correspondence.