Devicor Medical Products, Inc. Warehouse/Distribution/Service Center

FDA Device Registration & Listing · Blue Ash, OH, US · Registration 3010339638

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
3010339638
FEI Number
3010339638
Entity Name
Devicor Medical Products, Inc. Warehouse/Distribution/Service Center
City/State/Country
Blue Ash, OH, US
Establishment Address
4750 Lake Forest Dr Ste 120, Blue Ash, OH 45242, US
Establishment Type(s)
Remanufacture Medical Device
Owner / Operator
Devicor Medical Products, Inc. (Owner Number: 10033297)
Owner / Operator Contact Address
300 E-Business Way, Fifth Floor, Cincinnati, OH 45241, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Mammotome® Hand Held System Hydromark Mammotome revolve EX Mammotome AutoCore™ Single Insertion Core Biopsy System Mammotome® EX Hand Held System Mammotome Prima MR Dual Vacuum-Assisted Breast Biopsy System HydroMARK Plus Breast Biopsy Site Marker HydroMARK™ Plus Breast Biopsy Site Marker (Hummingbird Shape) Mammotome® MR Biopsy System HydroMark Breast Biopsy Site Marker Mammotome elite Biopsy System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2010-07-30
NEU Marker, Radiographic, Implantable General, Plastic Surgery Class 2 878.4300 2020-12-17
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2020-08-26
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2024-11-01
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2010-07-30
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2026-03-05
NEU Marker, Radiographic, Implantable General, Plastic Surgery Class 2 878.4300 2023-07-19
NEU Marker, Radiographic, Implantable General, Plastic Surgery Class 2 878.4300 2024-08-09
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2010-07-30
NEU Marker, Radiographic, Implantable General, Plastic Surgery Class 2 878.4300 2022-04-22
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2016-08-12

Official Correspondent

Katrine Austin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Devicor Medical Products, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3008992312 Devicor Medical Products de Mexico S de RL de CV Tijuana Baja California, MX
3008492462 DEVICOR MEDICAL PRODUCTS, INC. Cincinnati, OH, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K172344 Medax Srl Unipersonale Medax Biopsy Systems II (MEDONE, MEDCUT, MEDEM, MEDBONE, MEDLOCK) 2017-11-13

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2024 Bard Peripheral Vascular Inc 2
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Z-0028-2013 Remington Medical Inc. 2
Automatic Cutting Needles, Soft Tissue Biopsy Needle, NAC-1820M, Sterile, Remington Medical, Inc., 5830 Meadowridge Court, Alpharetta, GA 30005. Prostate Biopsy Needles shall be single use only and are to be used by a Urologist in a healthcare setting to obtain needle biopsies of the prostate. The needles are compatible with the Bard Magnum biopsy instrument. The needles have an echogenic tip for accurate placement under ultrasound guidance and centimeter markings along the cannula to facilitate depth placement.
Z-0042-2014 Atossa Genetics, Inc. 2
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity System Kits, MASCT Patient Sample Kits & Clarity Patient Sample Kits Instrument, Biopsy. The MASCT System Kit, Patient Sample Kits, or the Nipple Aspirate Fluid Laboratory Kit has the following codes: PRODUCT CODE: AG-MASCT; AG-FC5; DTG-MASCT, DTG-FC5, and NRLBH-5. PART NUMBER: 9002513; 9002513MD; 9002528; 9002528MD; 9002587; 9002614; and 9002717MD. THE MASCT SYSTEM KIT CONSISTS OF: 1. MASCT Breast Pump; 2. Instructions for Use (IFU); 3. Heating Pad; 4. Timer; 5. Saccomono's Fixative; 6. Nu Prep Gel; 7. Welcome and Training Materials Coversheet; 8. MASCT System Order Form; 9. ForeCYTE Training Video DVD; 10. MASCT System Instructions with pictures - pink; THE PATIENT SAMPLE KIT CONSISTS OF: 1. Two (2) flower assemblies (e.g., filter, filter retainer, and filter holder); 2. Instructions for Use (IFU); 3. Two (2) specimen collection devices; 4. Two (2) breast bags for transporting the specimen collection container; 5. Barcode labels; 6. Saccomono's Fixative; 7. Nu Prep Gel; 8. MASCT System package insert; 9. ForeCYTE Test Requisition Form; 10. Patient Information Sheet; 11. Atossa Patient Information; 12. FED EX Clinical PAK; 13. MASCT System Order Form; 14. FED EX Pouch; 15. FED EX Airbill; Product Usage: The MASCT Device is intended for use in the collection of nipple aspirate fluid for cytological testing. The collected fluid can be used in the determination and/or differentiation of normal versus premalignant versus malignant cells.
Z-0044-2018 Bard Peripheral Vascular Inc 2
BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18 g x 16 cm; MC1820, 18 g x 20 cm; MC1825, 18 g x 25 cm. The core needle biopsy device is intended for use in obtaining biopsies from soft tissues.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010339638. Last updated year: 2026. Please use registration number 3010339638 when referencing this establishment in official correspondence.
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