Apricity

FDA Device Registration & Listing · Appleton, WI, US · Registration 2133432

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
2133432
FEI Number
1000520824
Entity Name
Apricity
City/State/Country
Appleton, WI, US
Establishment Address
3901 W Spencer St, Appleton, WI 54914, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Apricity Services (Owner Number: 9019838)
Owner / Operator Contact Address
4764 W Integrity Way, suite 312, Appleton, WI 54913, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Motivo Tour Walker Coleman 200 Piece Expedition Kit Coleman All-Purpose Tin Coleman Fishing Essentials Tin Coleman 100 Piece Waterproof Kit Coleman Personal Survival Tin Coleman Outdoor Essentials Tin

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITJ Walker, Mechanical Physical Medicine Class 1 890.3825 2021-07-01
LRR First Aid Kit With Drug Unknown Class N N/A 2013-01-23

Official Correspondent

Dan Haak

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Apricity Services
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 2133432. Last updated year: 2026. Please use registration number 2133432 when referencing this establishment in official correspondence.
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