CORIT MEDICAL LLC

FDA Device Registration & Listing · McLean, VA, US · Registration 3025961941

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
3025961941
FEI Number
3025961941
Entity Name
CORIT MEDICAL LLC
City/State/Country
McLean, VA, US
Establishment Address
1765 Greensboro Station Place, Suite 900, McLean, VA 22102, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CorIT Medical LLC (Owner Number: 10087168)
Owner / Operator Contact Address
1765 Greensboro Station Place, Tower 1, Suite 900, McLean, VA 22102, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CORIT Turbinate Reduction Instrument

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRC Instrument, Ent Manual Surgical Ear, Nose, Throat Class 1 874.4420 2023-01-20

Official Correspondent

Aaron Tutwiler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CorIT Medical 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
K143738 Intuit Medical Products, LLC DSS Sinusplasty Balloon Catheter 2015-08-27

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025961941. Last updated year: 2026. Please use registration number 3025961941 when referencing this establishment in official correspondence.
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