Bexa, Inc.

FDA Device Registration & Listing · Pleasantville, NY, US · Registration 3020798169

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
3020798169
FEI Number
3020798169
Entity Name
Bexa, Inc.
City/State/Country
Pleasantville, NY, US
Establishment Address
427 Manville Rd, Suite 390A, Pleasantville, NY 10570, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Bexa, Inc. (Owner Number: 10057868)
Owner / Operator Contact Address
929 Deep Valley Dr, Rolling Hills Estates, CA 90274, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K181672
PMA Number
N/A

All Registered Proprietary Names

SureTouch Mobile Pressure Mapping System Bexa Pressure Mapping System Model 1885 Bexa Pressure Mapping System: device, stand, phantom and scale, case, charger(s), and optional tablet display

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NKA System, Documentation, Breast Lesion Obstetrics/Gynecology Class 2 884.2990 2019-07-30

Official Correspondent

David Ables

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bexa, 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 3020798169. Last updated year: 2026. Please use registration number 3020798169 when referencing this establishment in official correspondence.
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