D-KAT Z-Type

Catalogue number 2414-P-2010, listed by Keeler Ltd., United Kingdom, under Tonometer, Manual. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (2), Beijing (1), Shanghai (1).

Chinese manufacturers registered for FDA product code HKY
Manufacturer City Province Registered as Device types
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
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 D-KAT Z-Type
Listed by Keeler Ltd., United Kingdom
FDA product code HKY
Device type Tonometer, Manual
Device class Class 2
Regulation 21 CFR 886.1930
Establishment Contract manufacturer, Specification developer, Manufacturer
Record published 2016-03-21
Record revised 2023-02-06 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number

Catalogue Numbers

Catalogue numbers for D-KAT Z-Type
Catalogue number Size Status
2414-P-2010 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Tonometer AT 900 Haag-Streit AG 7
Ambler Surgical Ambler Surgical, LLC 7
Ocu-Film® +” Reichert Inc. 5
Bausch + Lomb Bausch & Lomb Incorporated 5
AccuTip Cover Accutome, Inc. 4
Mediworks Shanghai Mediworks Precision Instruments Co., Ltd. 4
Applanation Tonometer Chongqing Sunkingdom Medical Instrument Co., Ltd. 3
Icare ic200 Icare Finland Oy 3
Marco Takagi Seiko Co., Ltd. 2
S4 Optik Costruzioni Strumenti Oftalmici C.S.O. SRL 2
iCare PATIENT2 Icare Finland Oy 2
Tonometer AT 870 Haag-Streit AG 2

Showing 12 of 71. All products under Tonometer, Manual

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K152644 2015-12-31
K142179 2014-09-17
K133234 2014-02-21
K093445 2010-01-19

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