Bausch + Lomb

27 ga. Bi-Blade Vitreous Cutter Posterior Wide-Field Stellaris Elite Pack

Registry build 21.09.26
4manufacturers in China registered for this device type
109catalogue numbers in this listing
11510(k) clearances naming this product code
18recalls on this code

Who Else Makes It

Concentrated in Guangdong (2), Shanghai (1), Jiangsu (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HQC
Manufacturer City Province Registered as Device types
Sanmina Kunshan Jiangsu Contract manufacturer 15
Providence Enterprise Limited Shenzhen Guangdong Contract manufacturer 9
ABA Medical Technology Co Ltd Guang Dong Guangdong Contract manufacturer 6
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65

Record

Regulatory record for Bausch + Lomb
Listed by Bausch & Lomb Incorporated, United States
FDA product code HQC
Device type Unit, Phacofragmentation
Device class Class 2
Regulation 21 CFR 886.4670
Establishment Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-09-24
Record revised 2025-10-10 (version 13)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date, serial number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Bausch + Lomb
Catalogue number Size Per pack Status
DP8300 In distribution
BL5121 6 In distribution
SE5620AV 6 In distribution
BL5277 6 In distribution
SE14565E In distribution
DP8130 6 In distribution
BLV0000000 6 In distribution
SE5625BB+ 6 In distribution
BL5113 6 In distribution
BLS226TT30 6 In distribution
DP8330A In distribution
SE5627BB+ 6 In distribution
DP8215 In distribution
DP8315 In distribution
DP8930S 6 In distribution
ET4750 AP23 In distribution
DP8245S 6 In distribution
SE5425MV 6 In distribution
SE15565 In distribution
SE5427WVB 6 In distribution
BL3270 In distribution
MVS 1052 In distribution
DP8430S 6 In distribution
BL5277 In distribution
BLV322MM30 6 In distribution
DP5511 6 In distribution
MVS1083 In distribution
SE5423MVB 6 In distribution
BL3160 In distribution
SE5527WVB 6 In distribution
DP5200A 6 In distribution
DP8730S 6 In distribution
BL3318S 6 In distribution
SE5525MVB 6 In distribution
DP4310 6 In distribution
SE15565E In distribution
BLV3220000 6 In distribution
BL3420S 6 In distribution
BL5110 6 In distribution
DP8730 In distribution
BL3124 In distribution
DP5100 6 In distribution
BL5275 6 In distribution
BL3162 In distribution
BLV4180000 6 In distribution
BL3170 In distribution
BL3164 In distribution
BLV128MP30 6 In distribution
BL5114A 6 In distribution
DP8330S 6 In distribution
BL5120 6 In distribution
BL3420AS 6 In distribution
DP4305 12 In distribution
DP8030S 6 In distribution
BL3163 In distribution
BL5113A 6 In distribution
SE14565 In distribution
SE5625 6 In distribution
DP8330 In distribution
DP8145S 6 In distribution
BL3234 In distribution
CX9503 10 In distribution
SE5623AVBB+ 6 In distribution
D4600A 6 In distribution
BLS0000000 6 In distribution
SE5623AV 6 In distribution
DP8245 In distribution
BL5111 6 In distribution
BL5625S 6 In distribution
BL5123 6 In distribution
BL5123A 6 In distribution
DP8830AS 6 In distribution
DP8230 In distribution
SE5627B 6 In distribution
BL3166 In distribution
SE5525MV 6 In distribution
DP8430AS 6 In distribution
BL5114 6 In distribution
BL3124S 12 In distribution
BLP324MX30 6 In distribution
ET4753 A23 In distribution
BL3118 6 In distribution
DP8345 In distribution
CX4320 6 In distribution
ET4750 A23 In distribution
DP5531 6 In distribution
SE5523MV 6 In distribution
DP8930AS 6 In distribution
BL3318AS 6 In distribution
SE5427MVB 6 In distribution
BL3165 In distribution
MVS 1063 In distribution
BL5112 6 In distribution
BLP226MX30 6 In distribution
BL5280 6 In distribution
SE5520M 6 In distribution
MVS 1063C In distribution
DP8130S 6 In distribution
BLV2260000 6 In distribution
MVS 1061L In distribution
BL3161 In distribution
SE5425MVB 6 In distribution
BL5427MVXB 6 In distribution
DP5501 12 In distribution
DP8830S 6 In distribution
MVS 1063S In distribution
DP8230S 6 In distribution
SE5623BB+ 6 In distribution
BLV126MF30 6 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Alcon Alcon Laboratories, Inc. 95
Oertli® Oertli Instrumente AG 66
Laminar Johnson & Johnson Surgical Vision, Inc. 40
Engauge Alcon Laboratories, Inc. 18
Unity Alcon Laboratories, Inc. 18
Constellation Alcon Laboratories, Inc. 16
MST/Packard A1.7mm Phaco Tip Bent Dewey 30° Microsurgical Technology, Inc. 11
Whitestar Signature Johnson & Johnson Surgical Vision, Inc. 10
Alcon, Infiniti, MicroSmooth, ABS Alcon Laboratories, Inc. 10
Compact Intuitiv Johnson & Johnson Surgical Vision, Inc. 9
Alcon, Infiniti, Intrepid Alcon Laboratories, Inc. 9
MST.7mm A1 Bent Phaco Tip 45° Microsurgical Technology, Inc. 8

Showing 12 of 619. All products under Unit, Phacofragmentation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K170052 2017-04-19
K162342 2017-03-24
K133486 2014-03-12
K133242 2014-02-14
K101325 2010-08-17
K082473 2009-01-05
K082132 2008-08-28
K073023 2008-03-12
K063331 2006-12-19
K041998 2004-08-16
K033653 2003-12-17

Recalls Naming This Product

3 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Bausch + Lomb
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Bausch & Lomb Incorporated UDI-DI 2018-08-08 Class II Nonconforming Material/Component The back cap separates from the body of the vitrectomy cutter. 67 cases 2019-08-28
Bausch & Lomb Incorporated UDI-DI 2018-08-08 Class II Nonconforming Material/Component The back cap separates from the body of the vitrectomy cutter. 39.33 cases 2019-08-28
Bausch & Lomb Incorporated UDI-DI 2018-08-08 Class II Nonconforming Material/Component The back cap separates from the body of the vitrectomy cutter. 66 cases 2019-08-28

Recalls

1 of these is 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
2012-08-31 Class II Process control Posterior fluidics modules installed in the system may need to be recalibrated. 124 units 2013-07-11
2011-07-27 Not classified Nonconforming Material/Component The aspiration channel on the affected vacuum cassettes may be blocked due to a molding malfunction 229/6-unit cases 2013-06-21
2011-07-27 Not classified Nonconforming Material/Component The aspiration channel on the affected vacuum cassettes may be blocked due to a molding malfunction 6/6-unit cases 2013-06-21
2011-07-27 Not classified Nonconforming Material/Component The aspiration channel on the affected vacuum cassettes may be blocked due to a molding malfunction 9/6-unit cases 2013-06-21
2011-07-27 Not classified Nonconforming Material/Component The aspiration channel on the affected vacuum cassettes may be blocked due to a molding malfunction 2/6-unit cases 2013-06-21
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 280/6-pouch boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 7,256/12-pack boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 8,964/6-pack boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 308/6-pouch boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 1,958/6-pouch boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 6,111/6-pouch boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 286/6-pouch boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 233/6-pouch boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 783/6-pouch boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 2,282/6-pouch boxes 2012-04-02
2010-01-08 Not classified Component design/selection Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate 1,265/6-pack boxes 2012-04-02
2003-08-25 Not classified Other The firm’s DP8200 Microflow Needle Packs were labeled with the firm’s DP8115 Phaco Needle Packs and visa versa. 44 boxes 2003-12-15
2003-08-25 Not classified Other The firm’s DP8200 Microflow Needle Packs were labeled with the firm’s DP8115 Phaco Needle Packs and visa versa. 22 boxes 2003-12-15

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