SAUNDERS ELECTRONICS

FDA Device Registration & Listing · South Portland, ME, US · Registration 3013919529

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
3013919529
FEI Number
3013919529
Entity Name
SAUNDERS ELECTRONICS
City/State/Country
South Portland, ME, US
Establishment Address
192 Gannett Drive, South Portland, ME 04106, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Saunders Electronics (Owner Number: 10055706)
Owner / Operator Contact Address
192 Gannett Drive, South Portland, ME 04106, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Prapela SVS hospital bassinet pad

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QVY Therapeutic Vibrational Mattress Pad, Adjunct Use In Neonatal Abstinence Syndrome Or Neonatal Opioid Withdrawal Syndrome General Hospital Class 2 880.5151 2025-08-11

Official Correspondent

Paul Meserve

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Saunders Electronics
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 3013919529. Last updated year: 2026. Please use registration number 3013919529 when referencing this establishment in official correspondence.
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