REIA, LLC

FDA Device Registration & Listing · Portland, ME, US · Registration 3031738269

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
3031738269
FEI Number
3031738269
Entity Name
REIA, LLC
City/State/Country
Portland, ME, US
Establishment Address
411 Congress St, Portland, ME 04101, US
Establishment Type(s)
Repack or Relabel Medical Device,Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Reia, LLC (Owner Number: 10091085)
Owner / Operator Contact Address
331 River Road, Lyme, NH 03768, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Reia pessary Reia applicator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHW Pessary, Vaginal Obstetrics/Gynecology Class 2 884.3575 2024-06-27
HGD Applicator, Vaginal Obstetrics/Gynecology Class 1 884.4520 2024-06-27

Official Correspondent

Kaitlin Maier

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Reia, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K933654 Johnson & Johnson Medical, Inc. BLADDER NECK SUPPORT PROTHESIS FITTING KIT 1995-05-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031738269. Last updated year: 2026. Please use registration number 3031738269 when referencing this establishment in official correspondence.
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