Trademark Elevating Table
2 catalogue numbers from E9012-L, listed by Pivotal Health Solutions, United States, under Table, Powered. 13 manufacturers in China are registered for this product code.
13manufacturers in China registered for this device type
2catalogue numbers in this listing
Who Else Makes It
Concentrated in Jiangsu (6), Shanghai (2), Guangdong (2).
Showing 12 of 13. All 13 manufacturers in China registered for Table, Powered
Record
| Listed by | Pivotal Health Solutions, United States |
|---|---|
| FDA product code | INQ |
| Device type | Table, Powered |
| Device class | Class 1 |
| Regulation | 21 CFR 890.3760 |
| Establishment | Complaint-file establishment, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2021-08-27 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| E9012-L | In distribution | |
| E9212-L | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Clinton Industries | Clinton Industries, Inc | 218 |
| UMF Medical | United Metal Fabricators, Inc. | 187 |
| Armedica | Armedica Manufacturing Corp. | 153 |
| Coinfycare | Huangshan Jinfu Medical Equipment Co., Ltd. | 83 |
| Dynatronics | Armedica Manufacturing Corp. | 32 |
| Lifetec | Armedica Manufacturing Corp. | 24 |
| SCT 3000 | Pressalit A/S | 16 |
| Elite | Elite Manufacturing | 13 |
| EVERYWAY4ALL | Everyway Medical Instruments Co., Ltd. | 13 |
| Vario | Ropox A/S | 10 |
| Elevating Hand Therapy Table | Pivotal Health Solutions | 10 |
| SCT 2000 | Pressalit A/S | 9 |
Showing 12 of 275. All products under Table, Powered
Recalls Naming This Product
1 recall names this product by its own identifier, the UDI on its label.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Pivotal Health Solutions | UDI-DI | 2024-04-29 | Class II | Nonconforming Material/Component | This product is being recalled due to potentially insufficient rework on a part (E7130-B) on the lumbar section of the frame on 6 distributed tables. There were 4 additional tables with the faulty E7130-B part that were manufactured, but ha | 32 tables |
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.