BioSet®

RT Allograft Paste, Syringe, 0.5cc

Registry build 21.09.26
2manufacturers in China registered for this device type
47catalogue numbers in this listing
1510(k) clearance

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 BioSet®
Listed by Rti Surgical, Inc., United States
FDA product code MQV
Device type Filler, Bone Void, Calcium Compound
Device class Class 2
Regulation 21 CFR 888.3045
510(k) K043421
Record published 2015-11-06
Record revised 2023-10-19 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries expiry date, serial number
Storage Storage environment temperature -39 to -20 °C

Catalogue Numbers

Catalogue numbers for BioSet®
Catalogue number Size Status
008850 In distribution
015710 In distribution
807890 In distribution
806710 In distribution
008890 In distribution
006705 In distribution
005810 In distribution
006810 In distribution
005801 In distribution
805710 In distribution
015700 In distribution
807891 In distribution
006702 In distribution
015701 In distribution
005805 In distribution
007875 In distribution
016720 In distribution
007845 In distribution
806702 In distribution
807875 In distribution
006805 In distribution
807845 In distribution
006820 In distribution
007890 In distribution
016710 In distribution
016705 In distribution
806720 In distribution
005700 In distribution
005701 In distribution
806705 In distribution
015705 In distribution
016702 In distribution
018850 In distribution
005710 In distribution
005705 In distribution
005800 In distribution
007891 In distribution
007820 In distribution
007830 In distribution
006710 In distribution
807820 In distribution
805701 In distribution
807830 In distribution
805700 In distribution
018890 In distribution
805705 In distribution
006720 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
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
Cem-Ostetic Putty Berkeley Advanced Biomaterials 34

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
K241555 2025-02-21

Recalls Naming This Product

26 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of BioSet®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Exactech, Inc. 510(k) number 2019-04-26 Class II Environmental control The Opteform Disc-30mm, Opteform Disc-45mm, and Opteform Disc-90mm were potentially exposed to higher temperatures than those documented in the IFU due to a failure of the cold storage equipment. 2 units 2021-04-22
Exactech, Inc. 510(k) number 2019-04-26 Class II Environmental control The Opteform Disc-30mm, Opteform Disc-45mm, and Opteform Disc-90mm were potentially exposed to higher temperatures than those documented in the IFU due to a failure of the cold storage equipment. 2 units 2021-04-22
Exactech, Inc. 510(k) number 2019-04-26 Class II Environmental control The Opteform Disc-30mm, Opteform Disc-45mm, and Opteform Disc-90mm were potentially exposed to higher temperatures than those documented in the IFU due to a failure of the cold storage equipment. 3 units 2021-04-22
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2017-01-23 Class II Labeling Change Control Incorrect instructions for use (IFU) included. 24 units 2018-04-05
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2013-12-06 Class II Other RTI Surgical, Inc. of Alachua, FL is recalling their OPTEFORM Allograft Paste, 5cc as it may contain a 10 cc fluid dispenser. The 10cc fluid dispenser does not include the correct fluid fill line reference for reconstitution of 5cc past all 14 units 2014-09-15
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2011-04-09 Not classified Labeling mix-ups RTI Biologics issued a recall of Osteofil DBM Paste, 5cc that was distributed on 03/04/2008 to one customer. The product was labeled as 5.0cc but should have been labeled as 0.5cc. All customers were notified of this recall on 04/09/2011. 26 units 2012-07-24
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26
RTI Surgical, Inc. (dba RTI Biologics, Inc.) 510(k) number 2005-10-14 Not classified Other The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processin 2012-07-26

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