ATLAS INTL.

FDA Device Registration & Listing · RANCHO CORDOVA, CA, US · Registration 2951225

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
2951225
FEI Number
1000221494
Entity Name
ATLAS INTL.
City/State/Country
RANCHO CORDOVA, CA, US
Establishment Address
11389 Trade Center Dr, RANCHO CORDOVA, CA 95742, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
ATLAS INTL. (Owner Number: 9007577)
Owner / Operator Contact Address
11389 TRADE CENTER DR., --, Rancho Cordova, CA 95742, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Oscimed Cast Saw Hebu Cast Saw Stern Podia Exam Chair

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LGH Instrument, Cast Removal, Ac-Powered Orthopedic Class 1 888.5960 2021-08-09
FRK Chair, Examination And Treatment General Hospital Class 1 880.6140 2024-01-12

Official Correspondent

REBECA ROLFF

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ATLAS INTL.
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 2951225. Last updated year: 2026. Please use registration number 2951225 when referencing this establishment in official correspondence.
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