ImarC™

Tissue Marker System - Stereotactic Delivery

Registry build 21.09.26
1manufacturer
5catalogue numbers in this listing
6510(k) clearances naming this product code
1recall

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 ImarC™
Listed by Carbon Medical Technologies, Inc., United States
FDA product code NEU
Device type Marker, Radiographic, Implantable
Device class Class 2
Regulation 21 CFR 878.4300
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2015-09-24
Record revised 2023-09-18 (version 4)

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Carton of 10
Sizes Length 3 to 4 mm; outer diameter 1 to 2 mm
Distribution end date 2017-12-07
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for ImarC™
Catalogue number Size Status
040210 Length 4 mm Withdrawn
040303 Length 3 mm Withdrawn
040301 Length 4 mm Withdrawn
040201 Length 4 mm Withdrawn
040304 Length 4 mm Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
HydroMARK Devicor Medical Products, Inc. 75
Scout® Merit Medical Systems, Inc. 68
Scout MD™ Merit Medical Systems, Inc. 46
SmartClip Elucent Medical Inc. 37
BiomarC® Carbon Medical Technologies, Inc. 25
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
TriMark Hologic, Inc. 14

Showing 12 of 96. All products under Marker, Radiographic, Implantable

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K251748 2025-07-23
K132708 2013-12-20
K100994 2010-04-30
K070436 2007-03-16
K063193 2006-11-21
K042296 2004-09-20

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2022-12-16 Class II Under Investigation by firm The label incorrectly identifies the product as STAR1401, a 1x3mm Barbell shaped marker pre-loaded in a 14 gauge needle, while the packaging contains STAR1402, a 1x5mm Tribell shaped marker pre-loaded in a 14 gauge needle. 550 devices 2023-08-09

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