Tricut®

Blade 1884004HR Tricut 5PK M4 4MM Rotate

Registry build 21.09.26
5manufacturers in China registered for this device type
31catalogue numbers in this listing
1510(k) clearance
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Shandong (1), Hebei (1).

Chinese manufacturers registered for FDA product code EQJ
Manufacturer City Province Registered as Device types
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
Debo Medical Technology (Shijiazhuang) Co., Ltd. Shijiazhuang Hebei Contract manufacturer 117
Tribest Dental Products Co Ltd Yangzhong Jiangsu Contract manufacturer 58
Zonefly Medical Devices Co., Ltd. Danyang Jiangsu Specification developer 7
Guizhou Zirui Technology Co., Ltd. Tongzi County, Zunyi Guizhou Manufacturer 4

Record

Regulatory record for Tricut®
Listed by Medtronic Xomed, Inc., United States
FDA product code EQJ
Device type Bur, Ear, Nose And Throat
Device class Class 1
Regulation 21 CFR 874.4140
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2017-10-13
Record revised 2024-05-23 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Length 11 to 45 cm; outer diameter 2.9 to 4 mm; angle 15 °
Distribution end date 2023-12-06

Catalogue Numbers

Catalogue numbers for Tricut®
Catalogue number Size Per pack Status
1884004HR Length 11.0 cm 5 In distribution
1884004HRE Length 11.0 cm In distribution
1882904HRE Length 11.0 cm In distribution
1883504 Length 11.0 cm 5 In distribution
1882904 Outer Diameter 2.9 mm 5 In distribution
1884080HR Outer Diameter 4.0 mm 5 In distribution
1884035HRE Outer Diameter 4.0 mm In distribution
1882904 Length 11.0 cm 5 In distribution
1884035HRE Outer Diameter 4.0 mm In distribution
1884004 Length 11.0 cm 5 In distribution
1883504HR Length 11.0 cm 5 In distribution
1882904HRE Outer Diameter 2.9 mm In distribution
1884020 Outer Diameter 4.0 mm 3 In distribution
1884030 Outer Diameter 4.0 mm 3 In distribution
1884030HRE Angle 15.0 ° In distribution
1884020 Outer Diameter 4.0 mm 3 In distribution
1884004 Outer Diameter 4.0 mm 5 In distribution
1884004HR 5 In distribution
1884031HRE Outer Diameter 4.0 mm In distribution
1884031 Length 27.5 cm 3 In distribution
1884033HRE Outer Diameter 4.0 mm In distribution
1884080HRE Outer Diameter 4.0 mm In distribution
1883504HR 5 In distribution
1884030 Angle 15.0 ° 3 In distribution
1884030HRE Outer Diameter 4.0 mm In distribution
1884031HRE Length 27.0 cm In distribution
1884031 Outer Diameter 4.0 mm 3 In distribution
1883504 Outer Diameter 3.5 mm 5 In distribution
1884033HRE Angle 15.0 ° In distribution
1883504HRE Length 11.0 cm Withdrawn
1884004E Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Bur, Ear, Nose And Throat Medtronic Xomed, Inc. 413
Gyrus Acmi Gyrus Acmi, Inc. 99
Diego Elite Gyrus Acmi, Inc. 97
Jedmed Jedmed Instrument Company 88
Diego Gyrus Acmi, Inc. 56
RAD® Medtronic Xomed, Inc. 53
Invotec ENT Bur Invotec International, Inc. 50
NSK Sterile Burs/Drills Nakanishi Inc. 46
Wexler Surgical, Inc. Wexler Surgical, Inc. 41
Bur, Ear, Nose And Throat Karl Storz GmbH & Co. KG 39
Medline Medline Industries, Inc. 36
Bur, Ear, Nose And Throat Hager & Meisinger Gesellschaft mit beschränkter Haftung 30

Showing 12 of 646. All products under Bur, Ear, Nose And Throat

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K041985 2004-08-12

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Tricut®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Medtronic Xomed, Inc. UDI-DI 2021-08-31 Class II Process control There was an increase in complaints related to tip breaks and wobble/vibration. 274,991 total devices

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
2024-07-05 Class II Under Investigation by firm Product was distributed past expiration date. 1 unit
2002-01-25 Not classified Other Product packaging pouches may be open thereby compomising the sterile barrier. 120 2012-07-13

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