Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3039642990

FEI Number

3039642990

Entity Name

PERIMETRICS, INC

City/State/Country

Santa Ana, CA, US

Establishment Address

2961 W MacArthur Blvd, Suite 121, Santa Ana, CA 92704, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Perimetrics, Inc (Owner Number: 9058882)

Owner / Operator Contact Address

2961 W MacArthur Blvd, Ste 121, --, Santa Ana, CA 92704, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K232657

PMA Number

N/A

All Registered Proprietary Names

InnerView System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EKX	Handpiece, Direct Drive, Ac-Powered	Dental	Class 1	872.4200	2024-06-11

Official Correspondent

Alicia Mszyca

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Perimetrics, Inc

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K241065	Dentis Co., Ltd.	ChecQ (AC100)	2025-03-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039642990. Last updated year: 2026. Please use registration number 3039642990 when referencing this establishment in official correspondence.