SYNTECH, INT'L INC.

FDA Device Registration & Listing · IRVINE, CA, US · Registration 3005142514

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
3005142514
FEI Number
3005142514
Entity Name
SYNTECH, INT'L INC.
City/State/Country
IRVINE, CA, US
Establishment Address
17171 DAIMLER AVE., IRVINE, CA 92614, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
SYNTECH, INT'L INC. (Owner Number: 2083467)
Owner / Operator Contact Address
17171 DAIMLER AVE., --, Irvine, CA 92614, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tube Set Tube Set

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FYD Apparatus, Exhaust, Surgical General, Plastic Surgery Class 2 878.5070 2020-06-16
FYD Apparatus, Exhaust, Surgical General, Plastic Surgery Class 2 878.5070 2017-04-06

Official Correspondent

NICK HERBERT

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SYNTECH, INT'L INC.
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 3005142514. Last updated year: 2026. Please use registration number 3005142514 when referencing this establishment in official correspondence.
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