Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020857381

FEI Number

3020857381

Entity Name

PEDIAMETRIX INC

City/State/Country

Rockville, MD, US

Establishment Address

155 Gibbs St., Suite 537, Rockville, MD 20850, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

PediaMetrix Inc (Owner Number: 10083270)

Owner / Operator Contact Address

155 Gibbs St., Suite 537, Rockville, MD 20850, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K212045

PMA Number

N/A

All Registered Proprietary Names

SoftSpot

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QQO	Cranial Measurement Software	General, Plastic Surgery	Class 1	878.4800	2021-11-08

Official Correspondent

Reza Seifabadi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PediaMetrix Inc

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 3020857381. Last updated year: 2026. Please use registration number 3020857381 when referencing this establishment in official correspondence.