STRECK LLC

FDA Device Registration & Listing · La Vista, NE, US · Registration 3017953151

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
3017953151
FEI Number
3017953151
Entity Name
STRECK LLC
City/State/Country
La Vista, NE, US
Establishment Address
11710 Peel Circle, --, La Vista, NE 68128, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
STRECK (Owner Number: 1950302)
Owner / Operator Contact Address
7002 SOUTH 109TH ST., --, La Vista, NE 68128, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
DEN200001
PMA Number
N/A

All Registered Proprietary Names

Cyto-Chex BCT Guardant cfDNA BCT Cell-Free DNA BCT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GIM Tubes, Vacuum Sample, With Anticoagulant Clinical Chemistry Class 2 862.1675 2013-01-21
QMA Blood Collection Device For Cell-Free Nucleic Acid Clinical Chemistry Class 2 862.1676 2024-07-29
QMA Blood Collection Device For Cell-Free Nucleic Acid Clinical Chemistry Class 2 862.1676 2020-08-07

Official Correspondent

Wendy Royalty

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

STRECK
View consolidated registration, premarket clearance, and recall records for this applicant.
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Other Registrations for Same Entity

Registration Number Establishment Name Location
1950302 STRECK LLC La Vista, NE, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017953151. Last updated year: 2026. Please use registration number 3017953151 when referencing this establishment in official correspondence.
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