Falcon
The Falcon rotatable retrieval basket is used to retrieve foreign bodies, tissue specimens, stones or calculi in endoscopic procedures of the gastrointestinal tract.
2manufacturers in China registered for this device type
2catalogue numbers in this listing
Who Else Makes It
All of them in Shanghai.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Sterigenics Shanghai ETO Ltd. | Shanghai | Shanghai | Contract manufacturer | 65 |
| Innovex Medical Co., Ltd. | Shanghai | Shanghai | Manufacturer | 5 |
Record
| Listed by | Us Endoscopy, United States |
|---|---|
| FDA product code | FGO |
| Device type | Dislodger, Stone, Flexible |
| Device class | Class 2 |
| Regulation | 21 CFR 876.4680 |
| 510(k) | K962676 |
| Record published | 2020-03-19 |
| Record revised | 2021-04-07 (version 6) |
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 |
| Storage | Special storage condition: Keep Dry |
| Packaging | Case of 5, box of 5 |
| Sizes | Length 230 cm; width 35 mm; outer diameter 2.5 mm |
| Distribution end date | 2022-11-28 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 00711141 | Length 230 cm | Withdrawn |
| 00711141 | Width 35 mm | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Gyrus Acmi | Gyrus Acmi, Inc. | 41 |
| Dornier MedTech | Dornier Medtech America, Inc. | 13 |
| Olympus | Gyrus Acmi, Inc. | 7 |
| Dislodger, Stone, Flexible | Stryker GmbH | 5 |
| Talon | Us Endoscopy | 2 |
| USA Elite | Gyrus Acmi, Inc. | 2 |
| Stone Cone | Boston Scientific Corporation | 2 |
| Gyrus Icmi | Gyrus Acmi, Inc. | 1 |
| Stone Retrieval Basket | Applied Medical Resources Corp. | 1 |
| Soltive | Gyrus Acmi, Inc. | 1 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| United States Endoscopy Group, Inc. | 510(k) number | 2011-11-14 | Class II | Device Design | When the outer catheter is either coiled or in a contorted configuration outside of the endoscope and the patient, and excessive force is applied to the handle, the jaws may become inoperable and may become stuck in the open condition. | 1153 | 2013-07-02 |
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.