OmniSight™

OmniSight Passive Probe Set Sterilization Tray

Registry build 21.09.26
5manufacturers in China registered for this device type
6catalogue numbers in this listing
1510(k) clearance
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (1), Shandong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HAW
Manufacturer City Province Registered as Device types
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Sinovation (Beijing) Medical Technology Co., Ltd. Beijing Beijing Manufacturer 1

Record

Regulatory record for OmniSight™
Listed by Integra Lifesciences Corporation, United States
FDA product code HAW
Device type Neurological Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K010548
Record published 2016-08-25
Record revised 2024-04-05 (version 6)

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 lot or batch number, expiry date, manufacturing date, serial number
Packaging Box of 25
Distribution end date 2023-12-04

Catalogue Numbers

Catalogue numbers for OmniSight™
Catalogue number Size Status
OS4003 Withdrawn
OS7000 Withdrawn
OS4001 Withdrawn
OS4110 Withdrawn
OS4002 Withdrawn
OS2400L Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Neurological Stereotaxic Instrument Medtronic Navigation, Inc. 844
PMT Corporation – Stereotactic PMT Corp. 255
Leksell Stereotactic System Elekta Instrument AB 199
Neurological Stereotaxic Instrument Inomed Medizintechnik Gmbh 146
Neurological Stereotaxic Instrument Stryker Leibinger Gmbh & Co. KG 125
Geniant Cranial KOH Young Technology Inc. 113
CRW® Integra Lifesciences Corporation 107
Leksell Stereotactic System Elekta Solutions AB 93
microTargeting™ Insertion Tube with Stylet FHC, Inc. 60
Leksell Stereotactic System Neurosurgical Instruments Elekta Instrument AB 58
Leksell Vantage Stereotactic System Elekta Instrument AB 53
Stealth Autoguide™ System Medtronic Navigation, Inc. 50

Showing 12 of 1,137. All products under Neurological Stereotaxic Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K160811 2016-12-06

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. 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
2015-08-21 Class II Process design Integra identified that the UCHRAP component (Arc Adapter Plate) would not assemble properly to the UCHRAR component (ARC Adapter Ring) of the Compact Head Ring Adapter due to an error in the manufacturing drawing. 6 units 2016-10-13
2012-08-09 Class II Device Design T-handle screw is used on a complementary product to the CRW, the Integra HRAIM, which is the CT-compatible intubation Head Ring Assembly. When the T-handle on the HRAIM intubation hoop is tightened, the T-handle could stop in a vertical p 175 units 2014-03-26
2012-08-09 Class II Device Design T-handle screw is used on a complementary product to the CRW, the Integra HRAIM, which is the CT-compatible intubation Head Ring Assembly. When the T-handle on the HRAIM intubation hoop is tightened, the T-handle could stop in a vertical p 188 units 2014-03-26
2011-01-12 Not classified Manufacturing material removal Overall length of the intubation hoop in the HRAIM Intubation Head Ring Assembly is too long and will not allow a device to to attach 8 units 2011-04-04

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