SUMMIT LABS LLC

FDA Device Registration & Listing · Allegan, MI, US · Registration 3012544667

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
3012544667
FEI Number
3012544667
Entity Name
SUMMIT LABS LLC
City/State/Country
Allegan, MI, US
Establishment Address
605 N Eastern Ave, Allegan, MI 49010, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Summit Labs LLC (Owner Number: 10051661)
Owner / Operator Contact Address
605 N Eastern ave, Allegan, MI 49010, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DS2 Insole

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 2016-04-18

Official Correspondent

Jesse Henthorn

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Summit Labs LLC
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 3012544667. Last updated year: 2026. Please use registration number 3012544667 when referencing this establishment in official correspondence.
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