Triosite

Synthétic Bone Resorbable Graft Granules 2-4mm 16cc

Registry build 21.09.26
2manufacturers in China registered for this device type
15catalogue numbers in this listing
5510(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 Triosite
Listed by Biomatlante, France
FDA product code MQV
Device type Filler, Bone Void, Calcium Compound
Device class Class 2
Regulation 21 CFR 888.3045
Establishment Manufacturer
510(k) K051774
Record published 2016-05-11
Record revised 2023-02-01 (version 5)

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, manufacturing date
Distribution end date 2023-01-31
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Triosite
Catalogue number Size Status
00-0060-130-00 Granules 0.5-1mm 2cc Withdrawn
00-1109-115-02 Granules 2-4mm 16cc Withdrawn
00-1109-000-48 Wedge 8mm Withdrawn
00-1109-005-25 Disc Ø 25 ep 5mm Withdrawn
00-1109-000-36 Wedge 6mm Withdrawn
00-1109-132-15 Cone 12 Withdrawn
00-1109-005-03 Granules 2-3mm 5cc Withdrawn
00-1109-113-01 Sticks 5x5x10mm by 2 Withdrawn
00-1109-006-12 Wedge 12mm Withdrawn
00-1109-005-10 Wedge 10mm Withdrawn
00-1109-085-15 Cone 8 Withdrawn
00-1109-114-01 Sticks 5x5x20mm by 2 Withdrawn
00-1109-113-02 Sticks 5x5x10mm by 4 Withdrawn
00-1109-115-01 Granules 2-3mm 10cc Withdrawn
00-1109-114-02 Sticks 5x5x20mm by 4 Withdrawn

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
K071121 2007-09-11
K063527 2007-07-30
K051774 2006-01-20
K043005 2005-05-03
K032268 2003-12-11

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