KISMET HOLDINGS GROUP

FDA Device Registration & Listing · Hixson, TN, US · Registration 3016000960

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
3016000960
FEI Number
3016000960
Entity Name
KISMET HOLDINGS GROUP
City/State/Country
Hixson, TN, US
Establishment Address
2733 Kanasita Drive, Hixson, TN 37343, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Kismet Holdings Group (Owner Number: 10061334)
Owner / Operator Contact Address
10938 Hwy 58, Georgetown, TN 37336, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Walker

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITJ Walker, Mechanical Physical Medicine Class 1 890.3825 2019-10-09

Official Correspondent

Kismet Regulatory

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kismet Holdings Group
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 3016000960. Last updated year: 2026. Please use registration number 3016000960 when referencing this establishment in official correspondence.
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