Identity
- Trade Name
- EXOCEUTICALS FDA UDI
- Generic Name
- Hair growth laser device FDA UDI
- Device Name
- The Aduro Comb (Model: SZ-22A) is indicated to treat Androgenetic Alopecia and promote hair growth in males whohave Norwood- Hamilton Classifications of lla - V patterns of hair loss and to treat Androgenetic Alopecia and promotehair growth in females who have Ludwig-Savin Scale I-1 to -4. 1l-1. l-2 or ffontal patterns of hair loss: both with Fitzpatrick Skin Types I - IV. FDA UDI
- Model / Reference
- SZ-22A FDA UDI
- Description
- The Aduro Comb (Model: SZ-22A) is indicated to treat Androgenetic Alopecia and promote hair growth in males whohave Norwood- Hamilton Classifications of lla - V patterns of hair loss and to treat Androgenetic Alopecia and promotehair growth in females who have Ludwig-Savin Scale I-1 to -4. 1l-1. l-2 or ffontal patterns of hair loss: both with Fitzpatrick Skin Types I - IV. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850062024557 FDA UDI
- FDA Product Code
- OAP FDA UDI
- GMDN Term
- Hair growth laser device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Hair growth laser device
Exoceuticals by Shenzhen Kaiyan Medical Equipment Co, . Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Shenzhen Kaiyan Medical Equipment Co, . Ltd
Sources (1)
- FDA UDI b81a614c-5f81-4d3e-bfbb-7f1dbb471c58 33 fields · synced May 30, 2026