Cryoprobe D2.4 Mm/13g, 124 Mm, Trocar, Spheric.

Catalogue number FAP7600000, listed by Icecure Medical Ltd., Israel, under Unit, Cryosurgical, Accessories. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
4510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Guangdong (1), Beijing (1), Tianjin (1).

Chinese manufacturers registered for FDA product code GEH
Manufacturer City Province Registered as Device types
Shenzhen Kesite Digital Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 4
Hygea Medical Technology Co., Ltd. Beijing Beijing Manufacturer 2
Medinux (Tianjin) Technologies Co., Ltd. Tianjin Tianjin Manufacturer 1

Record

Regulatory record for Cryoprobe D2.4 mm/13G, 124 mm, Trocar, Spheric.
Listed by Icecure Medical Ltd., Israel
FDA product code GEH
Device type Unit, Cryosurgical, Accessories
Device class Class 2
Regulation 21 CFR 878.4350
Establishment Manufacturer
510(k) K183213
Record published 2019-10-24
Record revised 2024-07-11 (version 6)

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number
Storage Special storage condition: dry, cool, well-ventilated and clean environment without corrosive gas.
Packaging Shipper box
Sizes Shaft length 124 mm; needle gauge 13 G
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Cryoprobe D2.4 mm/13G, 124 mm, Trocar, Spheric.
Catalogue number Size Status
FAP7600000 Shaft Length 124 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Frigitronics Coopersurgical, Inc. 42
CryoProbe™ H&O Equipments, Nv/Sa 35
Wallach Coopersurgical, Inc. 32
Premier Premier Dental Products Co. 30
Hygea Hygea Medical Technology Co., Ltd. 26
truFreeze CSA Medical 20
Freezpen® H&O Equipments, Nv/Sa 19
Leisegang Cryotip for LM-900 Coopersurgical, Inc. 15
Integra® Miltex® Integra LifeSciences Production Corporation 13
cryoICE Cryoablation System Atricure, Inc. 13
CryoThin Medinux (Tianjin) Technologies Co., Ltd. 12
Erbe Erbe Elektromedizin GmbH 12

Showing 12 of 334. All products under Unit, Cryosurgical, Accessories

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K260377 2026-02-24
K240892 2024-06-28
K183213 2019-12-20
K102360 2010-11-29

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
2019-09-16 Class II Other Updated User Manual DSR3200000 Rev. E to include the safety guidelines in case of any mechanical damage (e.g. bent cryoprobe) 16 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