NexGraft
9 catalogue numbers from NBF1-90X22-10, listed by Berkeley Advanced Biomaterials, United States, under Filler, Bone Void, Calcium Compound. 2 manufacturers in China are registered for this product code.
2manufacturers in China registered for this device type
9catalogue numbers in this listing
14510(k) clearances naming this product code
1recall
Who Else Makes It
Concentrated in Shanghai (1), Beijing (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Zimmer (Shanghai) Medical International Trading Co., Ltd. | Shanghai | Shanghai | Exporter | 106 |
| Allgens Medical Technology Co., Ltd. | Beijing | Beijing | Complaint-file establishment | 1 |
Record
| Listed by | Berkeley Advanced Biomaterials, United States |
|---|---|
| FDA product code | MQV |
| Device type | Filler, Bone Void, Calcium Compound |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3045 |
| Establishment | Manufacturer |
| 510(k) | K092046 |
| Record published | 2016-04-08 |
| Record revised | 2020-10-19 (version 5) |
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, serial number |
| Distribution end date | 2016-12-05 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| NBF1-90X22-10 | Withdrawn | |
| NBF1-50X10-02 | Withdrawn | |
| NBF2-50X25-10 | Withdrawn | |
| NBF1-100X25-10 | Withdrawn | |
| NBF2-50X10-02 | Withdrawn | |
| NBF2-50X10-05 | Withdrawn | |
| NBF1-100X25-15 | Withdrawn | |
| NBF1-50X10-01 | Withdrawn | |
| NBF1-90X22-07 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Synthacer | medArtis Medizinprodukte und Forschung Aktiengesellschaft | 360 |
| Syntricer | medArtis Medizinprodukte und Forschung Aktiengesellschaft | 357 |
| Biosorb | S.B.M | 65 |
| MagnetOs | Kuros Biosciences B.V | 61 |
| BioSet® | Rti Surgical, Inc. | 47 |
| Bicera® Resorbable Bone Substitute | Wiltrom Corporation Limited | 41 |
| GRAFTON®and Grafton PLUS®Demineralized Bone Matrix (DBM) | Medtronic Sofamor Danek, Inc. | 40 |
| Bicera® Resorbable Bone Substitute | Wiltrom Co., Ltd. (Chutung) | 39 |
| ChronOS | Synthes Gmbh | 39 |
| Synthacer/Syntricer | medArtis Medizinprodukte und Forschung Aktiengesellschaft | 36 |
| Inion BioRestore™ | Inion OY | 35 |
| Resorba Synthetic Bone | Biomatlante | 35 |
Showing 12 of 750. All products under Filler, Bone Void, Calcium Compound
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K170917 | 2017-10-30 |
| K113791 | 2012-03-15 |
| K091912 | 2010-06-23 |
| K092046 | 2010-03-24 |
| K053213 | 2006-07-06 |
| K051914 | 2005-11-03 |
| K051695 | 2005-07-19 |
| K050666 | 2005-04-11 |
| K042636 | 2004-12-14 |
| K041889 | 2004-08-19 |
| K040405 | 2004-03-05 |
| K030266 | 2003-02-20 |
| K023703 | 2003-01-30 |
| K022622 | 2003-01-09 |
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 |
|---|---|---|---|---|
| 2025-09-02 | Class II | Process control | Due to incorrect product label (Incorrect product name identified on outer packaging). | 62 units |
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.