Who Else Makes It
Concentrated in Shanghai (1), Beijing (1). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Surgicel NU-Knit | Listed by | Ethicon Sàrl |
| FDA product code | LMG |
| Device type | Agent, Absorbable Hemostatic, Non-Collagen Based |
| Device class | Class 3 |
| Regulation | 21 CFR 878.4490 |
| 510(k) | N12159 |
| Record published | 2023-05-15 |
| Record revised | 2025-11-18 (version 14) |
Specifications
Specifications | MRI safety | MR Safe |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Storage environment temperature 59 to 86 °F; Storage environment temperature 15 to 30 °C |
| Packaging | Box of 12, case of 24, box of 10, case of 12, case of 10 |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
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.