THE MEDI-KID CO., INC.

FDA Device Registration & Listing · HEMET, CA, US · Registration 2032384

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
2032384
FEI Number
3003355294
Entity Name
THE MEDI-KID CO., INC.
City/State/Country
HEMET, CA, US
Establishment Address
448 SOUTH PALM, No. A, P.O.BOX 5398, HEMET, CA 92544, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
THE MEDI-KID CO., INC. (Owner Number: 9046155)
Owner / Operator Contact Address
448 S. PALM ST., #A, P.O. BOX 5398, Hemet, CA 92544, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

medi-wrap pedi-wrap

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2010-11-14

Official Correspondent

MELINDA SIWEK

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

THE MEDI-KID CO., INC.
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 2032384. Last updated year: 2026. Please use registration number 2032384 when referencing this establishment in official correspondence.
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