LEVISENSE MEDICAL, INC.

FDA Device Registration & Listing · Beverly, MA, US · Registration 3044677502

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
3044677502
FEI Number
3044677502
Entity Name
LEVISENSE MEDICAL, INC.
City/State/Country
Beverly, MA, US
Establishment Address
47 Enon St. - Unit 7, PMB 152, Beverly, MA 01915, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
LeviSense Medical, Inc. (Owner Number: 10095685)
Owner / Operator Contact Address
47 Enon St. - Unit 7, PMB 152, Beverly, MA 01915, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pro-Daptive SensorCell Flotation Surface

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FNM Mattress, Air Flotation, Alternating Pressure General Hospital Class 2 880.5550 2026-04-14

Official Correspondent

David Bertoni

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LeviSense Medical, 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 3044677502. Last updated year: 2026. Please use registration number 3044677502 when referencing this establishment in official correspondence.
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