Nova 5

The Fiducial Marker consists of a sealed polyether ether ketone (PEEK) polymer capsule containing a solution of up to 1.0% cobalt chloride and up to 2.0% N-Acetyl cysteine, in a ratio of…

Registry build 21.09.26

The Fiducial Marker consists of a sealed polyether ether ketone (PEEK) polymer capsule containing a solution of up to 1.0% cobalt chloride and up to 2.0% N-Acetyl cysteine, in a ratio of 1:2. Zirconium oxide is sealed within the device. The length of the polymer capsule is between 5.5 mm and 10.0 mm, and the diameter is 1.0 mm. It is loaded in an implant needle and sterilized with Ethylene Oxide.

1manufacturer
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code NEU
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106

Record

Regulatory record for Nova 5
Listed by C4 Imaging LLC, United States
FDA product code NEU
Device type Marker, Radiographic, Implantable
Device class Class 2
Regulation 21 CFR 878.4300
Establishment Specification developer, Manufacturer
510(k) K192771
Record published 2021-09-03
Record revised 2026-01-16 (version 4)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Nova 5
Catalogue number Size Status
F-01-03-0111 In distribution
F-01-03-0011 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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HydroMARK Breast Biopsy Site Marker Devicor Medical Products, Inc. 21
SecurMark Hologic, Inc. 15
Gold Marker Riverpoint Medical LLC 15
MammoStar™ Carbon Medical Technologies, Inc. 15
SecurMark for Atec Hologic, Inc. 15
SenoMark® Ultra Breast Tissue Marker Bard Peripheral Vascular, Inc. 14
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Showing 12 of 96. All products under Marker, Radiographic, Implantable

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K192771 2020-10-21

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer