Identity
- Trade Name
- GalaFLEX 3D FDA UDI
- Generic Name
- Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable FDA UDI
- Device Name
- GalaFLEX 3D Scaffold, 7.5 cm x 21.0 cm, Large Oval (Contents: 2) FDA UDI
- Model / Reference
- 100042-06 FDA UDI
- Description
- GalaFLEX 3D Scaffold, 7.5 cm x 21.0 cm, Large Oval (Contents: 2) FDA UDI
Identifiers
- Catalog Number
- SH3D06 FDA UDI
- Primary DI / UDI-DI
- 00810054980315 FDA UDI
- 510(k) Number
- K161092 FDA UDI
- FDA Product Code
- OOD FDA UDI
- GMDN Term
- Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 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
Dimensions & Sizes
- Size
- Height — 7.5 Centimeter FDA UDILength — 21.0 Centimeter FDA UDI
Category: Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable
GalaFLEX 3D by Tepha, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K161092 also covers:
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
- Tepha, Inc.
Sources (1)
- FDA UDI 36cd3917-96c5-40ee-aac8-22a0122ef3b6 38 fields · synced May 30, 2026