PROTO LABS

FDA Device Registration & Listing · Morrisville, NC, US · Registration 3038011210

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
3038011210
FEI Number
3038011210
Entity Name
PROTO LABS
City/State/Country
Morrisville, NC, US
Establishment Address
3615 Pleasant Grove Church Rd, Morrisville, NC 27560, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Proto Labs (Owner Number: 10093134)
Owner / Operator Contact Address
3615 Pleasant Grove Church Road, Morrisville, NC 27560, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QNN Prosthesis, Total Talus Replacement, Metal Unknown Class f N/A 2025-04-03

Official Correspondent

Jonathan Bissmeyer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Proto Labs
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 3038011210. Last updated year: 2026. Please use registration number 3038011210 when referencing this establishment in official correspondence.
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