Norian

Norian Drillable Fast SET Putty 10CC-STERILE

Registry build 21.09.26
2manufacturers in China registered for this device type
6catalogue 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 Norian
Listed by Synthes Gmbh, Switzerland
FDA product code MQV
Device type Filler, Bone Void, Calcium Compound
Device class Class 2
Regulation 21 CFR 888.3045
Establishment Specification developer, Manufacturer, Exporter
510(k) K073303
Record published 2015-09-14
Record revised 2026-05-21 (version 6)

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
Storage Storage environment temperature 5 to 25 °C; Handling environment temperature up to 43 °C; Special storage condition:.

Catalogue Numbers

Catalogue numbers for Norian
Catalogue number Size Status
07.704.010S In distribution
07.704.103S In distribution
07.704.110S In distribution
07.704.005S In distribution
07.704.003S In distribution
07.704.105S 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
K013072 2002-11-26

Recalls Naming This Product

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

Recalls naming the identifiers of Norian
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Synthes (USA) Products LLC 510(k) number 2017-08-10 Class II Process control The contract supplier notified DePuy Synthes on June 16, 2017 that the kit expiration dates do not align with the earliest expiration date of the component lots within the kit. Some kit expiration dates were later than the earliest expirati 5 units 2018-09-10
Synthes (USA) Products LLC 510(k) number 2016-05-11 Class II Under Investigation by firm DePuy Synthes is initiating a voluntary medical device recall of unexpired and unopened part and lot numbers for the Norian Drillable Injects-Sterile due to the rotary pouch within the referenced lots and associated part numbers may potenti 1246 units 2017-03-10
Synthes (USA) Products LLC 510(k) number 2016-05-11 Class II Under Investigation by firm DePuy Synthes is initiating a voluntary medical device recall of unexpired and unopened part and lot numbers for the Norian Drillable Injects-Sterile due to the rotary pouch within the referenced lots and associated part numbers may potenti 2812 units 2017-03-10
Synthes (USA) Products LLC 510(k) number 2016-05-11 Class II Under Investigation by firm DePuy Synthes is initiating a voluntary medical device recall of unexpired and unopened part and lot numbers for the Norian Drillable Injects-Sterile due to the rotary pouch within the referenced lots and associated part numbers may potenti 2098 units 2017-03-10

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