DIVERSILABS

FDA Device Registration & Listing · Jim Thorpe, PA, US · Registration 3008156050

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008156050
FEI Number
3008156050
Entity Name
DIVERSILABS
City/State/Country
Jim Thorpe, PA, US
Establishment Address
35 Autumn Lane, Jim Thorpe, PA 18229, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
DiversiLabs (Owner Number: 10031314)
Owner / Operator Contact Address
35 Autumn Lane, Jim Thorpe, PA 18229, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Dose Volume Histogram (DVH) Evaluat

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MUJ System, Planning, Radiation Therapy Treatment Radiology Class 2 892.5050 2010-01-14

Official Correspondent

Jimm Grimm

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DiversiLabs
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
K993675 Nomos Corp. PEREGRINE RADIATION THERAPY DOSE CALCULATION SYSTEM 2000-09-05

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0014-2012 Elekta, Inc. 2
Dynamic Multileaf Collimator (DMLC) Shapes the radiation beam in treatment therapy.
Z-0038-2017 RAYSEARCH LABORATORIES AB Sveavaegen 9 Stockholm Sweden 2
RayStation 2.5, 3.0, 3.5, 4.0, 4.5, 4.7, 5.0 and 4.3 (InverseArc 1.0) -- Radiation Therapy Treatment Planning System RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose distributions expected during the proposed treatment, and may be used to administer treatments after review and approval by the intended user. The system functionality can be configured based on user needs.

Similar Registrations

Registration Number Establishment Name Location
3004555507 EXTOL, INC Zeeland, MI, US
3025309924 SPECTRONIC MEDICAL AB Helsingborg Skane, SE
3014873236 ADAPTIIV MEDICAL TECHNOLOGIES, INC. Halifax Nova Scotia, CA
2916710 Varian Medical Systems, Inc PALO ALTO, CA, US
2030598 Synergy Health AST, LLC SAN DIEGO, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008156050. Last updated year: 2026. Please use registration number 3008156050 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.