KLI CORP.

FDA Device Registration & Listing · CARMEL, IN, US · Registration 1833694

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
1833694
FEI Number
1000115591
Entity Name
KLI CORP.
City/State/Country
CARMEL, IN, US
Establishment Address
484 E. Carmel Dr., #257, CARMEL, IN 46032, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
KLI CORP. (Owner Number: 9003711)
Owner / Operator Contact Address
484 E Carmel Dr, #257, Carmel, IN 46032, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ENTERTAINER'S SECRET THROAT RELIEF

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EPN Pump, Nebulizer, Manual Ear, Nose, Throat Class 1 874.5220 2001-11-26

Official Correspondent

David Schmitz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KLI CORP.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1833694. Last updated year: 2026. Please use registration number 1833694 when referencing this establishment in official correspondence.
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