Optefil® Allograft Paste, 10cc

Catalogue number 005010, listed by Rti Surgical, Inc., United States, under Filler, Bone Void, Calcium Compound. 2 manufacturers in China are registered for this product code.

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
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 Optefil® Allograft Paste, 10cc
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) K043420
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
Label carries lot or batch number, expiry date, serial number
Storage Storage environment temperature 1 to 37 °C

Catalogue Numbers

Catalogue numbers for Optefil® Allograft Paste, 10cc
Catalogue number Size Status
005010 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
K241555 2025-02-21

Recalls Naming This Product

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

Recalls naming the identifiers of Optefil® Allograft Paste, 10cc
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
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

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