Orise™ Gel
Submucosal lifting agent with needle.
3manufacturers in China registered for this device type
4catalogue numbers in this listing
1510(k) clearance
1recall
Who Else Makes It
Concentrated in Jiangsu (2), Shanghai (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Micro-Tech (Nanjing) Co., Ltd. | Nan Jing | Jiangsu | Contract manufacturer | 49 |
| Sterigenics Shanghai E Beam Ltd. | Shanghai | Shanghai | Contract manufacturer | 14 |
| Endoclot Plus Co., Ltd. | Suzhou | Jiangsu | Manufacturer | 5 |
Record
| Listed by | Boston Scientific Corporation, United States |
|---|---|
| FDA product code | PLL |
| Device type | Submucosal Injection Agent |
| Device class | Class 2 |
| Regulation | 21 CFR 876.1500 |
| Establishment | Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2018-10-22 |
| Record revised | 2024-06-19 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Packaging | Pack of 10 |
| Sizes | Total volume 10 ml |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| M00519210 | In distribution | |
| M00519230 | In distribution | |
| M00519200 | Total Volume 10 ml | In distribution |
| M00519220 | Total Volume 10 ml | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Eleview | Cosmo Technologies Ltd. | 3 |
| EverLift | GI Supply | 2 |
| BlueBoost(TM) Submucosal Injectable Solution | Micro-Tech (Nanjing) Co., Ltd. | 2 |
| EndoClot | Endoclot Plus Co., Ltd. | 2 |
| Blue Eye | THE Standard Co., Ltd. | 2 |
| EndoClot SIS | Endoclot Plus Co., Ltd. | 2 |
| LiftUp | Ovesco Endoscopy AG | 1 |
| Eleview 5mL | Cosmo Technologies Ltd. | 1 |
| Ascendo submucosal lifting agent | Us Endoscopy | 1 |
| Ascendo | Us Endoscopy | 1 |
| LiftUp Kit | Ovesco Endoscopy AG | 1 |
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K180068 | 2018-09-28 |
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.
| Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|
| 2022-10-10 | Class II | Under Investigation by firm | ***Update12/13/22***:Product removal due to higher incidence of adverse events of foreign body reactions*** Potential outcomes associated with foreign body reaction to remnant ORlSE Gel post procedure. Foreign body reaction which presented | 402,968 Total |
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.