Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1929340

FEI Number

1929340

Entity Name

JKR LABORATORIES, INC.

City/State/Country

WICHITA, KS, US

Establishment Address

10701 W Kellogg St, WICHITA, KS 67209, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

JKR LABORATORIES, INC. (Owner Number: 1929340)

Owner / Operator Contact Address

10701 WEST KELLOGG, Wichita, KS 67209, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

#102 XL Impression Syringe Handy Handle Red Handy Handle Blue #102S XL Spare Cylinder, Transparent

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCP	Syringe, Ent	Ear, Nose, Throat	Class 1	874.5220	2013-03-11

Official Correspondent

Lynette Sundeen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JKR LABORATORIES, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1929340. Last updated year: 2026. Please use registration number 1929340 when referencing this establishment in official correspondence.