Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042952037

FEI Number

3042952037

Entity Name

UPDOC

City/State/Country

Mountain View, CA, US

Establishment Address

851 Sierra Vista Ave, Unit A, Mountain View, CA 94043, US

Establishment Type(s)

Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

UpDoc (Owner Number: 10094835)

Owner / Operator Contact Address

851 Sierra Vista Ave, Unit A, Mountain View, CA 94043, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K253281

PMA Number

N/A

All Registered Proprietary Names

UpDoc Software

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NDC	Calculator, Drug Dose	Anesthesiology	Class 2	868.1890	2025-12-28

Official Correspondent

Kendal Dinsmore

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

UpDoc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3006400278	Picis Clinical Solutions, S.A.U.	BARCELONA, ES
3010817588	MEDICAL DECISION NETWORK	Charlottesville, VA, US
3017986070	BIOINTELLISENSE INC.	Golden, CO, US
3025343017	COMERGE AG	Zurich, CH
2032227	MEDTRONIC MINIMED	NORTHRIDGE, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042952037. Last updated year: 2026. Please use registration number 3042952037 when referencing this establishment in official correspondence.