WRYMARK, INC.

FDA Device Registration & Listing · Saint Louis, MO, US · Registration 3006074162

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
3006074162
FEI Number
3006074162
Entity Name
WRYMARK, INC.
City/State/Country
Saint Louis, MO, US
Establishment Address
11833 Westline Ind. Drive, Saint Louis, MO 63146, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Wrymark, Inc. (Owner Number: 10058841)
Owner / Operator Contact Address
11833 Westline Ind. Drive, Saint Louis, MO 63146, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

RESOURCE LABS WRYMARK PREMIUM ORTHOTICS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNP Orthosis, Corrective Shoe Physical Medicine Class 1 890.3475 2018-11-01

Official Correspondent

Tammy Weil

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Wrymark, 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 3006074162. Last updated year: 2026. Please use registration number 3006074162 when referencing this establishment in official correspondence.
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