Nanoss 3d Advanced Bone Graft Substitute

Advanced Bone Graft Substitute 10cc

Registry build 21.09.26
2manufacturers in China registered for this device type
4catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Shanghai (1), Beijing (1).

Chinese manufacturers registered for FDA product code MQV
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

Regulatory record for nanOss 3D Advanced Bone Graft Substitute
Listed by Xtant Medical Holdings, Inc., United States
FDA product code MQV
Device type Filler, Bone Void, Calcium Compound
Device class Class 2
Regulation 21 CFR 888.3045
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K132050
Record published 2024-04-16
Record revised 2025-04-07 (version 2)

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Handling environment temperature 1 to 37 °C

Catalogue Numbers

Catalogue numbers for nanOss 3D Advanced Bone Graft Substitute
Catalogue number Size Status
90-300-25508 In distribution
90-300-25504 In distribution
90-300-251008 In distribution
90-300-251004 In distribution

Same Product Code

Other products under the same FDA 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

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of nanOss 3D Advanced Bone Graft Substitute
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Xtant Medical Holdings, Inc. 510(k) number 2026-03-09 Class II Incorrect or no expiration date Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years. 225

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer