Rite Aid

Precision Freeze Wart Remover System

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
6510(k) clearances naming this product code
3recalls on this code

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 Rite Aid
Listed by Orasure Technologies, Inc., United States
FDA product code GEH
Device type Unit, Cryosurgical, Accessories
Device class Class 2
Regulation 21 CFR 878.4350
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2016-09-27
Record revised 2021-04-07 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Over the counter Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature up to 50 °C; Special storage condition: Protect from Sunlight
Packaging Pack of 6
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Rite Aid
Catalogue number Size Status
0361539 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
K060859 2006-07-18
K023487 2003-03-20
K990877 1999-06-14
K982358 1998-10-02
K980739 1998-05-26
K971392 1997-10-21

Recalls

3 of these are Class III. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2020-07-15 Class III Under Investigation by firm Unit boxes not properly sealed 3000 units 2022-03-14
2020-07-15 Class III Under Investigation by firm Unit boxes not properly sealed 23220 units 2022-03-14
2020-07-15 Class III Under Investigation by firm Unit boxes not properly sealed 23400 units 2022-03-14

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