Dermagold100

The OW100S is indicated to provide acoustic pressure shockwave in the treatment of chronic, full-thickness diabetic foot ulcer with wound area measuring no larger than 16 cm2, which extend…

Registry build 21.09.26

The OW100S is indicated to provide acoustic pressure shockwave in the treatment of chronic, full-thickness diabetic foot ulcer with wound area measuring no larger than 16 cm2, which extend through the epidermis, dermis, tendon, or capsule, but without bone exposure. The OW100S is indicated for adult (22 year and older), diabetic patients presenting with diabetic foot ulcers greater than 30 days in duration and is indicated for use in conjunction with standard diabetic ulcer care. The OW100S is indicated to provide acoustic pressure shockwaves in the treatment of superficial partial thickness second degree burns in adults (22 year or older). The OW100S is indicated for use in conjunction with standard of care burn treatment(s).

6manufacturers in China registered for this device type
2catalogue numbers in this listing

Who Else Makes It

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

Chinese manufacturers registered for FDA product code PZL
Manufacturer City Province Registered as Device types
E.M.S. Electro Medical Systems (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 2
Beijing Spiritlaser Science & Technology Co., Ltd. Beijing Beijing Contract manufacturer 21
Hebei Tuosite Technology Co., Ltd. Shijiazhuang Hebei Manufacturer 14
Beijing Perfectlaser Technology Co., Ltd. Beijing Beijing Manufacturer 12
Hebei Lufen Tech Co., Limited Xingtai Hebei Contract manufacturer 12
Sanhe Jumei Technology Co., Ltd. Sanhe Hebei Manufacturer 12

Record

Regulatory record for Dermagold100
Listed by MTS Medical AG, Germany
FDA product code PZL
Device type Extracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers
Device class Class 2
Regulation 21 CFR 878.4685
Establishment Manufacturer
510(k) K231710
Record published 2023-09-11
Record revised 2024-08-23 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Storage environment temperature 4 to 40 °C; Storage environment humidity 10 to 75 % RH; Storage environment atmospheric pressure 50 to 106 KiloPascal; Handling environment temperature 10 to 35 °C; Storage environment humidity 30 to 75 % RH; Storage environment atmospheric pressure 82 to 106 KiloPascal
Packaging Box
Sizes Weight 18 to 21 kg; depth 459 mm; width 400 mm; height 218 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Dermagold100
Catalogue number Size Status
OW100S-US Weight 21 kg In distribution
OW100-US Weight 18 kg In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
dermaPACE Applicator Sanuwave, Inc. 1
CS-Pro MED Curative Sound, LLC 1
dermaPACE System (Console with applicator) Sanuwave, Inc. 1
dermaPACE Console Sanuwave, Inc. 1
Softwave Gold Li MTS Medical AG 1

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