JUNA CORPORATION

FDA Device Registration & Listing · Wilmington, DE, US · Registration 3042067802

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
3042067802
FEI Number
3042067802
Entity Name
JUNA CORPORATION
City/State/Country
Wilmington, DE, US
Establishment Address
1209 N Orange St, Wilmington, DE 19801, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Juna Corporation (Owner Number: 10094291)
Owner / Operator Contact Address
1209 Orange Street, Wilmington, DE 19801, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Juna

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDC Instrument, Surgical, Disposable General, Plastic Surgery Class 1 878.4800 2025-11-21

Official Correspondent

Russell Moore

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Juna Corporation
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
K831798 I M, Inc. DISPOSABLE SCALPELS 1983-07-19

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042067802. Last updated year: 2026. Please use registration number 3042067802 when referencing this establishment in official correspondence.
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