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TEMPUS AI, Inc.

USA · Chicago

✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

n/aThis registry lists domestic registrants only

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

4listed device types

Class I 0Class II 3Class III 1

plus 4 registration records and 3 510(k), 4 PMA

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

0registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

0active device licences

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

pendingnot queried

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

pendingnot queried

RURussiaRoszdravnadzor

pendingnot queried

Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States4 registration records, 3 510(k), 4 PMA

Manufacturer names merged into this page: TEMPUS AI, Inc.

Business registration

CIK: 0001717115
Registration status: Active
Listing status: Listed (TEM)

Business registration data from SEC EDGAR, retrieved 2026-09-02. Public registry information only; details of directors and shareholders are not collected.

FDA 510(k) clearances by year

12024 · K233549

22025 · K241868

FDA listed device types

Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System 1Next Generation Sequencing Based Tumor Profiling Test 1Atrial Fibrillation Risk Prediction Machine Learning-Based Notification Software 1Reduced Ejection Fraction Machine Learning-Based Notification Software 1

Market	Identifier	Name	Class / date
US	K241868	xR IVD	2025-09-19
US	K250119	Tempus ECG-Low EF	2025-07-15
US	K233549	Tempus ECG-AF	2024-06-21

TEMPUS AI, Inc.

Registrations by market

How these numbers were verified

Company information

Business registration

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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