Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3025107383

FEI Number

3025107383

Entity Name

MEDICALOCK CORPORATION

City/State/Country

Ettrick, WI, US

Establishment Address

15833 W Judd Street, Ettrick, WI 54627, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

MedicaLock Corporation (Owner Number: 10086555)

Owner / Operator Contact Address

15833 W Judd Street, Ettrick, WI 54627, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SurgiLock 20" x 29" Torso Pad (one side) SurgiLock Tapered Leg Pad SurgiLock Jelly Wrap Positioning Kit SurgiLock Torso & Head Positioning Kit SurgiLock Jelly Wrap Long Positioning Kit SurgiLock Lateral Lumbar Interbody Fusion Positioning Kit SurgiLock Heel Positioner Kit SurgiLock 20" x 36" Striped Torso Pad SurgiLock Positioning Wedge Kit SurgiLock Traction Boot Liner SurgiLock Posterior Cervical Decompression and Fusion Positioning Kit SurgiLock 3 in 1 Head Positioner SurgiLock Anterior Cervical Discectomy Fusion Positioning Kit SurgiLock 59" Strap Pad SurgiLock 20" x 36" Torso Pad SurgiLock Lateral Thoracic Long Kit SurgiLock 20" x 24" Torso Pad (one side) SurgiLock 20" x 24" Torso Pad SurgiLock General Surgical Positioning Kit SurgiLock Robotics Positioning Kit SurgiLock Hip Kit SurgiLock Prone Lateral Interbody Fusion Positioning Kit SurgiLock 20" x 29" Torso Pad SurgiLock Lateral Thoracic Kit SurgiLock Trendelenburg Positioning Kit SurgiLock 24" x 6" Pad SurgiLock Standard Head Positioner CerviLock Strap Kit SurgiLock Trendelenburg Head Positioner SurgiLock Fracture Table Kit SurgiLock 8" x 10" Foam Pad SurgiLock GYN/Urology Positioning Kit SurgiLock SLS1016 SurgiLock SL1007 SurgiLock SL1016 SurgiLock SLS1007 Dentistry Lock Pad

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CCX	Support, Patient Position	Anesthesiology	Class 1	868.6820	2024-07-10
PUI	Drape, Surgical, Exempt	General, Plastic Surgery	Class 2	878.4370	2022-11-18
LRP	Tray, Surgical	General, Plastic Surgery	Class 1	878.4800	2024-07-30

Official Correspondent

Jodi Eide

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MedicaLock Corporation

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
K881095	CooperVision, Inc.	KOI(TM) INSTRUMENT TRAYS	1988-04-06

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0036-2010	Alphatec Spine, Inc.	1	ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.

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3007441485	MOSER-BAER AG	Sumiswald Bern, CH
3003495693	EMERALD NONWOVENS INTL. CO., LTD.	Phetchaburi, TH
3012226300	AVILIGN MEDICAL	Sialkot Punjab, PK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025107383. Last updated year: 2026. Please use registration number 3025107383 when referencing this establishment in official correspondence.