27g Ultra Short Vitrectomy Kit

Catalogue number 8310.27KS, listed by D.o.r.c. Dutch Ophthalmic Research Center (International) B.V., Netherlands, under Instrument, Vitreous Aspiration And Cutting, Ac-Powered. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number
3recalls on this code

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code HQE
Manufacturer City Province Registered as Device types
ABA Medical Technology Co Ltd Guang Dong Guangdong Contract manufacturer 6

Record

Regulatory record for 27G Ultra Short Vitrectomy Kit
Listed by D.o.r.c. Dutch Ophthalmic Research Center (International) B.V., Netherlands
FDA product code HQE
Device type Instrument, Vitreous Aspiration And Cutting, Ac-Powered
Device class Class 2
Regulation 21 CFR 886.4150
Establishment Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K190875
Record published 2019-06-04
Record revised 2020-03-19 (version 3)

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

Catalogue Numbers

Catalogue numbers for 27G Ultra Short Vitrectomy Kit
Catalogue number Size Status
8310.27KS In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Bausch + Lomb Bausch & Lomb Incorporated 108
Unity Alcon Laboratories, Inc. 47
Synergetics Synergetics USA, Inc. 44
Bi-Blade® Medical Instrument Development Laboratories, Inc. 28
Instrument, Vitreous Aspiration And Cutting, Ac-Powered Medical Instrument Development Laboratories, Inc. 21
Alcon Alcon Laboratories, Inc. 14
Constellation Alcon Laboratories, Inc. 9
Stellaris Bausch & Lomb Incorporated 6
EVA Nexus™ Posterior 25G TDC Pack D.o.r.c. Dutch Ophthalmic Research Center (International) B.V. 4
EVA Nexus™ Posterior 23G TDC Pack D.o.r.c. Dutch Ophthalmic Research Center (International) B.V. 4
EVA Nexus™ Posterior 27G TDC Pack D.o.r.c. Dutch Ophthalmic Research Center (International) B.V. 4
Engauge, Vektor Alcon Laboratories, Inc. 3

Showing 12 of 65. All products under Instrument, Vitreous Aspiration And Cutting, Ac-Powered

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
2026-04-30 Class II Process design An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. 2068 boxes totaling 12408 units
2026-04-30 Class II Process design An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. 261 boxes totaling 1566 units
2026-04-30 Class II Process design An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. 314 boxes, totaling 1884 units

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