Sorrento Bioglass 12cc (100 X 20 X 6 Mm)

Sorrento BioGlass is a resorbable bone void filler for surgically created or traumatic defects in the extremities and pelvis. It is intended for gaps that are not essential to the stability…

Registry build 21.09.26

Sorrento BioGlass is a resorbable bone void filler for surgically created or traumatic defects in the extremities and pelvis. It is intended for gaps that are not essential to the stability of the bone. This configuration supplies a 12 cc strip measuring 100 by 20 by 6 mm.

The strip contains beta tricalcium phosphate granules and bioactive glass dispersed through a porous type I bovine collagen matrix. After placement, the material is resorbed and replaced by bone during the healing process.

Preparation and Supply

The material must be wetted with bone marrow aspirate before use. It is supplied sterile in double peel packaging and is intended for a single use.

2manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

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 Sorrento Bioglass 12cc (100 x 20 x 6 mm)
Listed by Xenco Medical LLC, 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, Complaint-file establishment, Manufacturer
510(k) K173933
Record published 2026-04-13

Specifications

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

Catalogue Numbers

Catalogue numbers for Sorrento Bioglass 12cc (100 x 20 x 6 mm)
Catalogue number Size Status
HB-118-0012 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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K191074 2019-09-27
K173933 2018-09-13

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