MAST KEYSTONE, INC.

FDA Device Registration & Listing · RENO, NV, US · Registration 1926420

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1926420
FEI Number
1000161291
Entity Name
MAST KEYSTONE, INC.
City/State/Country
RENO, NV, US
Establishment Address
2200 Dickerson Rd, RENO, NV 89503, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MAST KEYSTONE, INC. (Owner Number: 1926420)
Owner / Operator Contact Address
2200 DICKERSON RD., --, Reno, NV 89503, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mast Keystone

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HLP Target, Fusion And Stereoscopic Ophthalmic Class 1 886.1880 1992-07-21

Official Correspondent

GIFFORD MAST

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MAST KEYSTONE, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1926420. Last updated year: 2026. Please use registration number 1926420 when referencing this establishment in official correspondence.
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