MAINSPRING MEDICAL LLC

FDA Device Registration & Listing · Martinez, GA, US · Registration 3011821164

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
3011821164
FEI Number
3011821164
Entity Name
MAINSPRING MEDICAL LLC
City/State/Country
Martinez, GA, US
Establishment Address
205 New Petersburg Dr Ste B, Martinez, GA 30907, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Mainspring Medical LLC (Owner Number: 10049800)
Owner / Operator Contact Address
205 New Petersburg Dr Ste B, Martinez, GA 30907, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Vacurect

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LKY Device, External Penile Rigidity Gastroenterology, Urology Class 2 876.5020 2015-08-07

Official Correspondent

Donald Lechner

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mainspring Medical 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 3011821164. Last updated year: 2026. Please use registration number 3011821164 when referencing this establishment in official correspondence.
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