Sureform

45mm Straight Tip Stapler

Registry build 21.09.26
16manufacturers in China registered for this device type
12catalogue numbers in this listing
2recalls on this code

Who Else Makes It

Concentrated in Shanghai (5), Jiangsu (5), Zhejiang (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code GDW
Manufacturer City Province Registered as Device types
Hangzhou Fushan Medical Appliance Co., Ltd. Hangzhou Zhejiang Contract manufacturer 44
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Zhangjiagang Municipal Cnnc Huakang Radiation Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 17
Covidien Medical Products (Shanghai) Manufacturing LLC Shanghai Shanghai Contract manufacturer 8
Beijing Biosis Healing Biological Technology Co., Ltd. Beijing Beijing Manufacturer 7
B.j.zh.f.panther Medical Equipment Co., Ltd. Beijing Beijing Manufacturer 6
Touchstone International Medical Science Co., Ltd. Suzhou Jiangsu Manufacturer 5
Sinolinks Medical Innovation, Inc. Changzhou Jiangsu Complaint-file establishment 5
Victor Medical Instruments Co., Ltd. Changzhou Jiangsu Manufacturer 5
Lucky Star Lrradiation Science Co., Ltd. Shanghai Shanghai Shanghai Contract manufacturer 5
Fengh Medical Co., Ltd. Jiangyin Jiangsu Manufacturer 4
Medtronic (Shanghai) Medical Technology Co., Ltd. Min Hang District Shanghai Specification developer 4

Showing 12 of 16. All 16 manufacturers in China registered for Staple, Implantable

Record

Regulatory record for Sureform
Listed by Intuitive Surgical, Inc., United States
FDA product code GDW
Device type Staple, Implantable
Device class Class 2
Regulation 21 CFR 878.4750
Establishment Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2022-05-11
Record revised 2020-03-02 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Box of 12, box of 6
Sizes Depth 2 to 30 mm; outer diameter 8 to 14 mm; length 30 to 45 mm

Catalogue Numbers

Catalogue numbers for Sureform
Catalogue number Size Status
488530 Outer Diameter 8 mm In distribution
48230M Depth 30 mm In distribution
48360G Depth 4.3 mm In distribution
48345T Depth 4.6 mm In distribution
48345G Depth 4.3 mm In distribution
48345M Depth 2 mm In distribution
480545 Outer Diameter 14 mm In distribution
480445 Outer Diameter 14 mm In distribution
436502 Length 45 mm In distribution
48360W Depth 2.5 mm In distribution
48360B Depth 3.5 mm In distribution
48360T Depth 5 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Endo GIA Covidien LP 51
Aeon Lexington Medical, Inc. 48
Proximate Ethicon Endo-Surgery, Inc. 42
Tri-Staple 2.0 Covidien LP 42
EEA Covidien LP 37
Echelon Endopath Ethicon Endo-Surgery, Inc. 33
Reloading Unit for Endo Linear Cutter Stapler B.j.zh.f.panther Medical Equipment Co., Ltd. 28
GIA Covidien LP 24
easyEndoTM Universal Linear Cutting Stapler and Loading Units for Single Use Ezisurg Medical Co., Ltd. 23
Circular Stapler B.j.zh.f.panther Medical Equipment Co., Ltd. 23
Endopath Ethicon Endo-Surgery, Inc. 22
Signia Covidien LP 19

Showing 12 of 105. All products under Staple, Implantable

Recalls Naming This Product

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

Recalls naming the identifiers of Sureform
Recalled by Identified by Initiated FDA class Root cause Reason
Intuitive Surgical, Inc. UDI-DI 2026-03-11 Class I Under Investigation by firm Reloads for curved-tipped stapler may potentially produce an incomplete staple line.

Recalls

2 of these are 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
2018-04-23 Class II Nonconforming Material/Component Intuitive Surgical, Inc. (ISI) has recently become aware of an issue with the da Vinci Xi Stapler 45 Blue and Green Reloads that may be missing a component of the knife mechanism. Without this component, the reload knife will not move and c 7337 2020-07-15
2018-04-23 Class II Nonconforming Material/Component Intuitive Surgical, Inc. (ISI) has recently become aware of an issue with the da Vinci Xi Stapler 45 Blue and Green Reloads that may be missing a component of the knife mechanism. Without this component, the reload knife will not move and c 6816 2020-07-15

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