COAST PNEUMATICS, INC.

FDA Device Registration & Listing · Anaheim, CA, US · Registration 3003476474

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
3003476474
FEI Number
3003476474
Entity Name
COAST PNEUMATICS, INC.
City/State/Country
Anaheim, CA, US
Establishment Address
8055 E Crystal Drive, Anaheim, CA 92807, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Coast Pneumatics, Inc. (Owner Number: 10083808)
Owner / Operator Contact Address
8055 E Crystal Drive, Anaheim, CA 92807, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOJ Indicator, Physical/Chemical Sterilization Process General Hospital Class 2 880.2800 2026-01-20
FRC Indicator, Biological Sterilization Process General Hospital Class 2 880.2800 2026-01-20
FRC Indicator, Biological Sterilization Process General Hospital Class 2 880.2800 2021-12-21

Official Correspondent

Harry Ellis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Coast Pneumatics, 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
K151482 Bcr Diagnostics, Inc. BCR-30-min BI™ and RBIP-ST30™ Readout Accessory 2016-02-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2007 N/A 2
3M Comply 1248 Gas Plasma Chemical Indicator Strips for use in STERRAD 100, STERRAD 100S and STERRAD 50 Sterilization Systems. Indicator for hydrogen peroxide sterilant.

Similar Registrations

Registration Number Establishment Name Location
3007412809 STERIS Corporation FRANKLIN PARK, IL, US
2410251 PROPPER MFG. CO., INC. Long Island City, NY, US
3009968482 HU-FRIEDY MFG CO., LLC Des Plaines, IL, US
3013298431 VEENAK INTERNATIONAL LIMITED BIRMINGHAM, GB
1417592 MEDLINE INDUSTRIES, LP - Northfield Northfield, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003476474. Last updated year: 2026. Please use registration number 3003476474 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.