JOINT JACK COMPANY

FDA Device Registration & Listing · Farmington, CT, US · Registration 1000159372

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
1000159372
FEI Number
1000159372
Entity Name
JOINT JACK COMPANY
City/State/Country
Farmington, CT, US
Establishment Address
220 Farmington Ave Ste 1, Farmington, CT 06032, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Joint Jack Company (Owner Number: 10047857)
Owner / Operator Contact Address
220 Farmington Ave, Ste 1, Farmington, CT 06032, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Joint Jack Company LLC Joint Jack Company LLC Joint Jack Company LLC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILH Splint, Hand, And Components Physical Medicine Class 1 890.3475 2014-11-07
ION Exerciser, Non-Measuring Physical Medicine Class 1 890.5370 2014-11-07
FQM Bandage, Elastic General Hospital Class 1 880.5075 2014-11-07

Official Correspondent

Karen Mastella

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Joint Jack Company
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 1000159372. Last updated year: 2026. Please use registration number 1000159372 when referencing this establishment in official correspondence.
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