Surgical Glide

Placement of intraocular lens into the posterior chamber. Also protects iris from prolapse or trauma during surgical procedures. Thickness 6 mil. End radius 1.5 mm.

Registry build 21.09.26
1manufacturer
1catalogue number

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code KYB
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235

Record

Regulatory record for Surgical Glide
Listed by Hurricane Medical, United States
FDA product code KYB
Device type Lens, Guide, Intraocular
Device class Class 1
Regulation 21 CFR 886.4300
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2020-05-05
Record revised 2022-12-08 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Radiation Sterilization, Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Length 25 mm; width 3 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Surgical Glide
Catalogue number Size Per pack Status
9201 Length 25 mm 50 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Duckworth & Kent Duckworth AND Kent Limited 5
Unfolder Emerald Johnson & Johnson Surgical Vision, Inc. 3
Monarch® II Alcon Laboratories, Inc. 2
MSI Precision Specialty Instruments MED Saver, Inc. 2
Unfolder Silver Johnson & Johnson Surgical Vision, Inc. 2
Monarch® III Alcon Laboratories, Inc. 2
IOL Manipulator – Sinskey Hurricane Medical 2
Lens Exchange Sytem Visioncare Ophthalmic Technologies Ltd. 2
Viscoject 1.8 Injector Set Medicel AG 1
Bausch + Lomb Bausch & Lomb Incorporated 1
Nucleus Chopper – P. Koch Hurricane Medical 1
Unfolder Platinum 1 Series Johnson & Johnson Surgical Vision, Inc. 1

Showing 12 of 18. All products under Lens, Guide, Intraocular

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