Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016592693

FEI Number

3016592693

Entity Name

DIMENSIONAL BIOCERAMICS, LLC

City/State/Country

Santa Cruz, CA, US

Establishment Address

2161 Delaware Avenue, Suite A, Santa Cruz, CA 95060, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

DImensional Bioceramics (Owner Number: 10062613)

Owner / Operator Contact Address

306 Turnberry Ct, Lebanon, IN 46052, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K182742

PMA Number

N/A

All Registered Proprietary Names

CRANIOSCULPT-FLOW DB-Cranial CRANIOSCULPT-C

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GXP	Methyl Methacrylate For Cranioplasty	Neurology	Class 2	882.5300	2020-02-20

Official Correspondent

Patsy Trisler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DImensional Bioceramics

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 3016592693. Last updated year: 2026. Please use registration number 3016592693 when referencing this establishment in official correspondence.