Syntech Development & Manufacturing

FDA Device Registration & Listing · Chino, CA, US · Registration 3008280537

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
3008280537
FEI Number
3008280537
Entity Name
Syntech Development & Manufacturing
City/State/Country
Chino, CA, US
Establishment Address
13948 Mountain Ave, Chino, CA 91710, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Syntech Development & Manufacturing/Nelson (Owner Number: 10042856)
Owner / Operator Contact Address
13948 Mountain Ave, Chino, CA 91710, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

KYZ / SYRINGE, IRRIGATING (NON DENTAL) D370522 SYRINGE, IRRIGATING (NON DENTAL)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYZ Syringe, Irrigating (Non Dental) General Hospital Class 1 880.6960 2020-01-24

Official Correspondent

Staci Nelson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Syntech Development & Manufacturing/Nelson
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 3008280537. Last updated year: 2026. Please use registration number 3008280537 when referencing this establishment in official correspondence.
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