Kasios TCP

22 catalogue numbers from K43112W, listed by Kasios, 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
22catalogue 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 Kasios TCP
Listed by Kasios, United States
FDA product code MQV
Device type Filler, Bone Void, Calcium Compound
Device class Class 2
Regulation 21 CFR 888.3045
Record published 2017-02-12
Record revised 2018-03-29 (version 2)

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, serial number

Catalogue Numbers

Catalogue numbers for Kasios TCP
Catalogue number Size Status
K43112W Wedge 12° In distribution
K43114C Diameter 14 mm Height 20 In distribution
K43108C Diameter 8 mm Height 20 In distribution
K43125B 25 x 25 x 25 mm In distribution
K43100G 1 cm³ In distribution
K43106W Wedge 6° In distribution
K43105G 5 cm³ In distribution
K43108W Wedge 8° In distribution
K43120B 15 x 15 x 20 mm In distribution
K43114W Wedge 14° In distribution
K43130B 15 x 20 x 30 mm In distribution
K43110G 10 cm³ In distribution
K43110W Wedge 10° In distribution
K43101G 1 cm³ In distribution
K43120G 20 cm³ In distribution
K43130G 30 cm³ In distribution
K43112C Diameter 12 mm Height 20 In distribution
K43110C Diameter 10 mm Height 20 In distribution
K43110U 10 cm³ In distribution
K43105R 5x5x20 mm X5 In distribution
K43102G 2 cm³ In distribution
K43115G 15 cm³ 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
K073214 2009-12-01

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