OSHA REVIEW, INC.

FDA Device Registration & Listing · Rancho Cordova, CA, US · Registration 3011061109

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
3011061109
FEI Number
3011061109
Entity Name
OSHA REVIEW, INC.
City/State/Country
Rancho Cordova, CA, US
Establishment Address
11306 Sunco Dr Ste 7, Rancho Cordova, CA 95742, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
OSHA Review, Inc. (Owner Number: 10047255)
Owner / Operator Contact Address
11306 Sunco Drive Ste 7, Rancho Cordova, CA 95742, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K905425
PMA Number
N/A

All Registered Proprietary Names

OSHA Review's Spore Check System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRC Indicator, Biological Sterilization Process General Hospital Class 2 880.2800 2020-02-25

Official Correspondent

Morgan Lawson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OSHA Review, 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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011061109. Last updated year: 2026. Please use registration number 3011061109 when referencing this establishment in official correspondence.
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