Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021038030

FEI Number

3021038030

Entity Name

JAM-LABS CORP

City/State/Country

Fremont, CA, US

Establishment Address

4121 Clipper Ct, Fremont, CA 94538, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

JAM-Labs Corp (Owner Number: 10083562)

Owner / Operator Contact Address

4121 Clipper Court, Fremont, CA 94538, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ORION RACK SKYTRON ASCEND IP VOIRELITE SURGICAL DISPLAY

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OUG	Medical Device Data System	General Hospital	Class 1	880.6310	2022-06-17
FWC	Camera, Television, Surgical, With Audio	General, Plastic Surgery	Class 1	878.4160	2021-12-01

Official Correspondent

John Thomas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JAM-Labs Corp

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 3021038030. Last updated year: 2026. Please use registration number 3021038030 when referencing this establishment in official correspondence.