DYAD ENTERPRISE LLC

FDA Device Registration & Listing · King of Prussia, PA, US · Registration 3017067307

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
3017067307
FEI Number
3017067307
Entity Name
DYAD ENTERPRISE LLC
City/State/Country
King of Prussia, PA, US
Establishment Address
1075 First Avenue, King of Prussia, PA 19406, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Dyad Enterprise LLC (Owner Number: 10075779)
Owner / Operator Contact Address
1075 First Ave, King of Prussia, PA 19406, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DYAD

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NNK Container, Specimen Mailer And Storage, Non-Sterile Pathology Class 1 864.3250 2020-06-26

Official Correspondent

Mark Bartosh

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dyad Enterprise LLC
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 3017067307. Last updated year: 2026. Please use registration number 3017067307 when referencing this establishment in official correspondence.
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