Identity
- Trade Name
- MINT LIFT FDA UDI
- Generic Name
- Lift thread, bioabsorbable FDA UDI
- Model / Reference
- MINT-I 18WC1810 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809779587536 FDA UDI
- 510(k) Number
- K220549 FDA UDI
- FDA Product Code
- NEW FDA UDI
- GMDN Term
- Lift thread, bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4840 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Category: Lift thread, bioabsorbable
Mint Lift by Hans Biomed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Lift thread, bioabsorbable.
- Silhouette Instalift — Sinclair Pharma US Inc. · Class II
- Silhouette Instalift — Sinclair Pharma US Inc. · Class II
- Silhouette Instalift — Sinclair Pharma US Inc. · Class II
- MINT — Hans Biomed Corporation · Class II
- MINT — Hans Biomed Corporation · Class II
- MINT — Hans Biomed Corporation · Class II
- MINT — Hans Biomed Corporation · Class II
- MINT LIFT — Hans Biomed Corporation · Class II
Cleared under the same submission
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hans Biomed Corporation
Sources (1)
- FDA UDI 4a1cbe35-7d85-47c4-a932-0b958f9d992a 33 fields · synced Jun 8, 2026