DICK MEDICAL SUPPLY

FDA Device Registration & Listing · COLUMBUS, OH, US · Registration 3005831263

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
3005831263
FEI Number
3005831263
Entity Name
DICK MEDICAL SUPPLY
City/State/Country
COLUMBUS, OH, US
Establishment Address
1946 Camaro Avenue, COLUMBUS, OH 43207, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
DICK MEDICAL SUPPLY, LLC (Owner Number: 9090179)
Owner / Operator Contact Address
1946 Camaro Avenue, Columbus, OH 43207, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DMS Advanced Medical Packaging Padded Board Splint Passive Limb Restraint STRETCHER STRAP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OKU Emergency Obstetrical Kit Obstetrics/Gynecology Class 1 884.4520 2024-01-08
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2016-12-29
FMQ Restraint, Protective General Hospital Class 1 880.6760 2016-12-29
FMR Device, Transfer, Patient, Manual General Hospital Class 1 880.6785 2006-07-25

Official Correspondent

DAVID DICK

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DICK MEDICAL SUPPLY, LLC
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
K962327 Sekure Seat Corp. SEKURE SEAT ADULT PASSIVE RESTRAINING DEVICE 1997-03-06
K963243 Heelbo, Inc. HEELBO BLAZER SLEEVED JACKET 1996-10-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005831263. Last updated year: 2026. Please use registration number 3005831263 when referencing this establishment in official correspondence.
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