Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017486146

FEI Number

3017486146

Entity Name

DISRUPTIVE MEDTECH, LLC

City/State/Country

Laramie, WY, US

Establishment Address

3821 Beech St, Laramie, WY 82070, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Disruptive MedTech, LLC (Owner Number: 10077918)

Owner / Operator Contact Address

3821 Beech St, Laramie, WY 82070, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PanPlasty Probe MACI Instrument Tray Accu-Joint Hemi Implant Tray Delta-Cast Serene Cast Remover Disruptive MedTech Cutters SmartShot PanPlasty Frame Accu-Joint Hemi Implant Accu-joint Hemi Implant Single Sterile Disruptive MedTech Mallets PanPlasty Trocar

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HXB	Probe	Orthopedic	Class 1	888.4540	2024-03-25
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2022-06-23
LGH	Instrument, Cast Removal, Ac-Powered	Orthopedic	Class 1	888.5960	2024-03-28
FZT	Cutter, Surgical	General, Plastic Surgery	Class 1	878.4800	2025-09-26
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2020-10-05
KWD	Prosthesis, Toe, Hemi-, Phalangeal	Orthopedic	Class 2	888.3730	2021-06-03
HXL	Mallet	General, Plastic Surgery	Class 1	878.4800	2025-09-26
HXI	Passer, Wire, Orthopedic	Orthopedic	Class 1	888.4540	2024-03-25

Official Correspondent

David Rechberger

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Disruptive MedTech, LLC

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105

Similar Registrations

Registration Number	Establishment Name	Location
2134947	GAUTHIER BIOMEDICAL, INC.	Grafton, WI, US
3004215117	MILLENNIUM SURGICAL CORP	Schaumburg, IL, US
1421879	PHOENIX INSTRUMENTS, INC.	Lisle, IL, US
3010155661	Synergy Health Sterilisation UK Ltd	Thorne Doncaster, GB
3015516266	Depuy Ireland UC	Co. Cork Munster, IE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017486146. Last updated year: 2026. Please use registration number 3017486146 when referencing this establishment in official correspondence.