CENOVA AB

FDA Device Registration & Listing · MJOLBY Ostergotland, SE · Registration 3005216725

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
3005216725
FEI Number
3005216725
Entity Name
CENOVA AB
City/State/Country
MJOLBY Ostergotland, SE
Establishment Address
4, FLORETTGATAN, MJOLBY Ostergotland 595 43, SE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
CENOVA AB (Owner Number: 9043892)
Owner / Operator Contact Address
4, FLORETTGATAN, --, MJOLBY, SE-NOTA 595 43, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AprioCore plus SeeStar Sterile Surtex Ponto bone anchored hearing system Morrison Ponto bone anchored hearing system Bonopty BA210 Abutment Tracer set; OTS Hip; OTS Hip Solution Emphasys; OTS Hip Solution Pinnacle; BI300 Implant Forsvall biopsy needle Ponto bone anchored hearing system OSI200 Implant Template Gangi Ponto bone anchored hearing system Ponto bone anchored hearing system GI Biopsy Instrument

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HXY Brace, Drill Orthopedic Class 1 888.4540 2017-06-27
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2020-03-13
GDF Guide, Needle, Surgical General, Plastic Surgery Class 1 878.4800 2017-06-27
ELR Post, Root Canal Dental Class 1 872.3810 2021-12-08
LXB Hearing Aid, Bone Conduction Ear, Nose, Throat Class 2 874.3302 2014-12-19
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2017-06-27
MAH Hearing Aid, Bone Conduction, Implanted Ear, Nose, Throat Class 2 874.3302 2016-09-19
GAA Needle, Aspiration And Injection, Disposable General, Plastic Surgery Class 1 878.4800 2005-06-21
LXB Hearing Aid, Bone Conduction Ear, Nose, Throat Class 2 874.3302 2013-01-16
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2025-12-10
LXB Hearing Aid, Bone Conduction Ear, Nose, Throat Class 2 874.3302 2013-01-16
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2025-06-10
MAH Hearing Aid, Bone Conduction, Implanted Ear, Nose, Throat Class 2 874.3302 2016-09-19
LRC Instrument, Ent Manual Surgical Ear, Nose, Throat Class 1 874.4420 2025-04-22
FCG Biopsy Needle Gastroenterology, Urology Class 2 876.1075 2019-01-02
MAH Hearing Aid, Bone Conduction, Implanted Ear, Nose, Throat Class 2 874.3302 2016-09-19
MAH Hearing Aid, Bone Conduction, Implanted Ear, Nose, Throat Class 2 874.3302 2021-12-08
FCG Biopsy Needle Gastroenterology, Urology Class 2 876.1075 2025-12-10

Official Correspondent

Jeanette Erbay

US Agent Details

Elisa Maldonado-Holmertz Business: Obelix Consulting Email: elisamh@obelixconsult.com Phone: (512) 4316069

Related Public Records

Same Entity

CENOVA AB
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
K172344 Medax Srl Unipersonale Medax Biopsy Systems II (MEDONE, MEDCUT, MEDEM, MEDBONE, MEDLOCK) 2017-11-13
K781371 Ferris Mfg. Corp. BONE MARROW ASPIRATION KIT 1978-09-20
K260601 Blue Belt Technologies, Inc. REAL INTELLIGENCE™ CORI™ 2026-03-26
K143738 Intuit Medical Products, LLC DSS Sinusplasty Balloon Catheter 2015-08-27
K150891 Covidien, LLC( Formerly Beacon Endoscopic Corp.) BNX Fine Needle Aspiration System and SharkCore LG Fine Needle Biopsy System 2015-05-01

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.
Z-0017-2023 Hobbs Medical, Inc. 1
Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005216725. Last updated year: 2026. Please use registration number 3005216725 when referencing this establishment in official correspondence.
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