PRECISION CAST PLASTIC PARTS, INC.

FDA Device Registration & Listing · Redding, CA, US · Registration 3032870

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
3032870
FEI Number
3002816805
Entity Name
PRECISION CAST PLASTIC PARTS, INC.
City/State/Country
Redding, CA, US
Establishment Address
2415 Larkspur Lane, Unit A, Redding, CA 96002, US
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
PRECISION CAST PLASTIC PARTS, Inc. (Owner Number: 9038752)
Owner / Operator Contact Address
7725 Camino Del Encina Dr, --, Redding, CA 96001, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PRECISION PROBE TUBES

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EWO Audiometer Ear, Nose, Throat Class 2 874.1050 1999-08-19

Official Correspondent

CHARLES CREIGHTON

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PRECISION CAST PLASTIC PARTS, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K780270 Maico Hearing Instruments, Inc. COMPUTER AUDIOMETER - MA26 1978-02-27
K923074 Life-Tech Intl., Inc. DANPLEX SCREENING AUDIOMETER 1992-09-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032870. Last updated year: 2026. Please use registration number 3032870 when referencing this establishment in official correspondence.
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