Callos

Callos Impact Bone Void Filler Mixing and Delivery System for Acumed

Registry build 21.09.26
2manufacturers in China registered for this device type
15catalogue numbers in this listing
6510(k) clearances naming this product code
24recalls on this 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 Callos
Listed by Skeletal Kinetics, LLC, United States
FDA product code MQV
Device type Filler, Bone Void, Calcium Compound
Device class Class 2
Regulation 21 CFR 888.3045
Record published 2015-10-30
Record revised 2021-03-22 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 15 to 30 °C
Sizes Total volume 3 to 25 ml
Distribution end date 2021-01-01
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Callos
Catalogue number Size Status
65-0110-S Total Volume 10 ml Withdrawn
CALL-0005 Total Volume 5 ml Withdrawn
CALL-0003 Total Volume 3 ml Withdrawn
CALL-0105 Total Volume 5 ml Withdrawn
65-0003-S Total Volume 3 ml Withdrawn
CALL-JE10 Total Volume 10 ml Withdrawn
CALL-0110 Total Volume 10 ml Withdrawn
65-0010-S Total Volume 10 ml Withdrawn
CALL-PA10 Total Volume 10 ml Withdrawn
CALL-PA25 Total Volume 25 ml Withdrawn
CALL-PA05 Total Volume 5 ml Withdrawn
65-0005-S Total Volume 5 ml Withdrawn
65-0105-S Total Volume 5 ml Withdrawn
CALL-JE05 Total Volume 5 ml Withdrawn
CALL-0010 Total Volume 10 ml Withdrawn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
K132211 2014-08-04
K120354 2013-03-21
K112383 2012-02-07
K100986 2010-07-20
K051123 2005-06-03
K030554 2003-05-20

Recalls

24 of these are Class II. Class II means a temporary or reversible health consequence. 1 is recorded with the root cause “No Marketing Application”: the device was distributed without the premarket submission its class requires, a compliance finding rather than a defect. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 62 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 379 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 35 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 217 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 101 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 442 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 20 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 491 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 41 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 86 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 121 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 150 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 375 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 12 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 60 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 1 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 184 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 1053 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 15 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 88 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 21 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 4 2021-02-24
2020-04-06 Class II Under Investigation by firm Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include inc 40 2021-02-24
2015-05-29 Class II No Marketing Application Reports of venous uptake, DVT, pulmonary embolism in patients who were implanted with Injection Plasty Bone Void Filler. 67 kits 2015-07-24

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