Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009974364

FEI Number

3009974364

Entity Name

PRECISION IDENTITY CORP. / KAMBER

City/State/Country

Campbell, CA, US

Establishment Address

804 Camden Ave., Campbell, CA 95008, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Precision Identity Corp. / Kamber (Owner Number: 10042368)

Owner / Operator Contact Address

804 Camden Ave., Campbell, CA 95008, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

probe

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HXB	Probe	Orthopedic	Class 1	888.4540	2013-01-18

Official Correspondent

Roland Kamber

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Precision Identity Corp. / Kamber

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 3009974364. Last updated year: 2026. Please use registration number 3009974364 when referencing this establishment in official correspondence.