RINOVUM SUBSIDIARY 2, LLC

FDA Device Registration & Listing · Export, PA, US · Registration 3015417614

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
3015417614
FEI Number
3015417614
Entity Name
RINOVUM SUBSIDIARY 2, LLC
City/State/Country
Export, PA, US
Establishment Address
4923 Simmons Circle, Export, PA 15632, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Rinovum Subsidiary 2, LLC (Owner Number: 10060129)
Owner / Operator Contact Address
4923 Simmons Circle, Export, PA 15632, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K183468
PMA Number
N/A

All Registered Proprietary Names

Revive

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHW Pessary, Vaginal Obstetrics/Gynecology Class 2 884.3575 2019-04-02

Official Correspondent

Stephen Bollinger

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Rinovum Subsidiary 2, 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 3015417614. Last updated year: 2026. Please use registration number 3015417614 when referencing this establishment in official correspondence.
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