IOLMaster 700

The IOLMaster 700 is intended for biometric measurements and visualization of ocular structures. The measurements and visualization assist in the determination of the appropriate power and…

Registry build 21.09.26

The IOLMaster 700 is intended for biometric measurements and visualization of ocular structures. The measurements and visualization assist in the determination of the appropriate power and type of intraocular lens. The IOLMaster 700 measures: • Lens thickness • Corneal curvature and thickness • Axial length • Anterior chamber depth • Pupil diameter • White-to-white distance (WTW) For visualization, the IOLMaster 700 employs optical coherence tomography (OCT) to obtain two-dimensional images of ocular structures of the anterior and posterior segments of the eye. The Reference Image functionality is intended for use as a preoperative and postoperative image capture tool.

7manufacturers in China registered for this device type
1catalogue number
9510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Chongqing (2), Beijing (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code HJO
Manufacturer City Province Registered as Device types
Chongqing Kanghua Ruiming S&T Co., Ltd. Chongqing Chongqing Contract manufacturer 3
Beijing Hongdee Corporation Beijing Beijing Private-label distributor 43
Taizhou City K&W International Trade Co., Ltd. Jiangyan Jiangsu Repacker / relabeller 38
Lianyungang Tiannuo Optical Instrument Co., Ltd. Lianyungang Jiangsu Contract manufacturer 31
66 Vision Tech Co., Ltd. Suzhou Jiangsu Private-label distributor 24
Shanghai Mediworks Precision Instruments Co., Ltd. Shanghai Shanghai Contract manufacturer 13
Chongqing Sunkingdom Medical Instrument Co., Ltd. Chongqing Chongqing Manufacturer 11

Record

Regulatory record for IOLMaster 700
Listed by Carl Zeiss Meditec Inc, United States
FDA product code HJO
Device type Biomicroscope, Slit-Lamp, Ac-Powered
Device class Class 2
Regulation 21 CFR 886.1850
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer
Record published 2016-07-10
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Latex Labelled latex-free
Label carries manufacturing date, serial number
Storage Storage environment humidity 10 to 95 % RH; Storage environment temperature -10 to 55 °C; Handling environment humidity 30 to 90 % RH; Handling environment temperature 10 to 35 °C

Catalogue Numbers

Catalogue numbers for IOLMaster 700
Catalogue number Size Status
IOLMaster 700 Weight: approx. 27 kg In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
MediWorks Shanghai Mediworks Precision Instruments Co., Ltd. 30
S4 Optik Costruzioni Strumenti Oftalmici C.S.O. SRL 24
Marco Takagi Seiko Co., Ltd. 17
Gilras U.S. Ophthalmic, L.L.C. 16
Visionix Luneau Technology Operations 15
LED Slit Lamp Right MFG. Co., Ltd. 13
Tiannuo / Tnmed Lianyungang Tiannuo Optical Instrument Co., Ltd. 12
Eli Ezer U.S. Ophthalmic, L.L.C. 12
Inami Inami & Co., Ltd. 11
Zoom Slit Lamp Right MFG. Co., Ltd. 8
Slit Lamp BQ 900 Haag-Streit AG 8
PolyLock Small Bone Fusion Orthopedics, LLC 7

Showing 12 of 168. All products under Biomicroscope, Slit-Lamp, Ac-Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K173771 2018-08-24
K162684 2017-05-31
K170171 2017-04-06
K161607 2017-02-23
K143275 2015-07-10
K141068 2014-09-09
K133476 2014-02-12
K122418 2013-04-12
K101182 2010-11-03

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of IOLMaster 700
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Carl Zeiss Meditec AG (Jena) UDI-DI 2018-06-25 Class II Employee error Calibration setting was incorrectly entered during manufacturing causing the optical coherence tomography (OCT) to obtain the incorrect two-dimensional images of ocular structures of the anterior and posterior segments of the eye. 1 2021-01-15

Recalls

2 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
2013-10-23 Class II Software in the Use Environment The user database delivered for download contained an erroneous value. Specifically the “aO” constant of the lens AMO Sensar AR40E is listed as “0.0” in the internal lens database of the IOLMaster. The correct value is -2.420. This could le 4,907 units 2014-04-17
2013-10-23 Class II Software in the Use Environment The user database delivered for download contained an erroneous value. Specifically the “aO” constant of the lens AMO Sensar AR40E is listed as “0.0” in the internal lens database of the IOLMaster. The correct value is -2.420. This could le 1,201 units 2014-04-17

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