SpyGlass™ Discover

SpyGlass™ Discover Retrieval Basket

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
6510(k) clearances naming this product code
9recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Zhejiang (2).

Chinese manufacturers registered for FDA product code LQR
Manufacturer City Province Registered as Device types
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Jiangsu Vedkang Medical Science and Technology Co., Ltd. Changzhou Jiangsu Manufacturer 20
Hangzhou AGS MedTech Co., Ltd. Hangzhou Zhejiang Repacker / relabeller 19
Scivita Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 19
Zhejiang Soudon Medical Technology Co., Ltd. Hangzhou Zhejiang Manufacturer 9

Record

Regulatory record for SpyGlass™ Discover
Listed by Boston Scientific Corporation, United States
FDA product code LQR
Device type Dislodger, Stone, Biliary
Device class Class 2
Regulation 21 CFR 876.5010
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2021-06-07

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, expiry date
Sizes Length 120 cm; outer diameter 0.8 mm

Catalogue Numbers

Catalogue numbers for SpyGlass™ Discover
Catalogue number Size Status
M00542990 Length 120 cm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
eyeMAX(TM) Extraction Basket Micro-Tech (Nanjing) Co., Ltd. 35
Single-use Extraction Baskets Scivita Medical Technology Co., Ltd. 18
Extraction Basket Micro-Tech (Nanjing) Co., Ltd. 15
Memory Cook Incorporated 10
Memory Basket Cook Incorporated 6
Stonetome Boston Scientific Corporation 6
Single Use 3-Lumen Extraction Balloon V Olympus Medical Systems Corp. 5
Single Use Retrieval Basket V Olympus Medical Systems Corp. 4
Dislodger, Stone, Biliary Hangzhou AGS MedTech Co., Ltd. 4
Cook Cook Incorporated 3
CardioFIT Karl Storz GmbH & Co. KG 2
VedBasket, Stone Extraction Baskets Jiangsu Vedkang Medical Science and Technology Co., Ltd. 2

Showing 12 of 22. All products under Dislodger, Stone, Biliary

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K203322 2021-05-26
K191789 2019-07-25
K071066 2007-06-29
K946358 1995-04-11
K925879 1993-02-08
K925495 1992-12-23

Recalls

The FDA has not published a severity grade for these. 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
2009-01-08 Not classified Packaging The ultraviolet light barrier on the pouch may be discolored, which will allow ultraviolet light into the package and may cause the latex retrieval balloon to become brittle and to leak or burst when inflated. 294 of all products. 2009-10-22
2009-01-08 Not classified Packaging The ultraviolet light barrier on the pouch may be discolored, which will allow ultraviolet light into the package and may cause the latex retrieval balloon to become brittle and to leak or burst when inflated. 294 of all products. 2009-10-22
2009-01-08 Not classified Packaging The ultraviolet light barrier on the pouch may be discolored, which will allow ultraviolet light into the package and may cause the latex retrieval balloon to become brittle and to leak or burst when inflated. 294 of all products. 2009-10-22
2006-05-19 Not classified Other Lack of assurance of sterility, as the sterile barrier may fail. 2007-06-20
2006-05-19 Not classified Other Lack of assurance of sterility, as the sterile barrier may fail. 2007-06-20
2006-05-19 Not classified Other Lack of assurance of sterility, as the sterile barrier may fail. 2007-06-20
2006-05-19 Not classified Other Lack of assurance of sterility, as the sterile barrier may fail. 2007-06-20
2006-05-19 Not classified Other Lack of assurance of sterility, as the sterile barrier may fail. 2007-06-20
2006-05-19 Not classified Other Lack of assurance of sterility, as the sterile barrier may fail. 2007-06-20

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