GalaSHAPE 3d
GalaSHAPE 3D scaffold is a bioresorbable surgical mesh manufactured from poly-4-hydroxybutyrate (P4HB).
1manufacturer
14catalogue numbers in this listing
11510(k) clearances naming this product code
1recall
Who Else Makes It
Registered in Fujian.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Xiamen MK Health Care Product Co., Ltd. | Xiamen | Fujian | Manufacturer | 7 |
Record
| Listed by | Tepha, Incorporated, United States |
|---|---|
| FDA product code | OOD |
| Device type | Surgical Film |
| Device class | Class 2 |
| Regulation | 21 CFR 878.3300 |
| Establishment | Specification developer, Manufacturer |
| Record published | 2016-09-02 |
| Record revised | 2025-09-17 (version 7) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Ethylene Oxide |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Sizes | Length 2.5 to 21 cm; height 5.3 to 10.2 cm; width 2.5 to 20.3 cm; outer diameter 7.6 cm |
| Distribution end date | 2020-09-25 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 100042-12 | Height 10.2 cm | Withdrawn |
| 100042-02 | Height 5.3 cm | Withdrawn |
| 100042-04 | Height 6.4 cm | Withdrawn |
| 100042-09 | Width 7.6 cm | Withdrawn |
| 100042-13 | Outer Diameter 7.6 cm | Withdrawn |
| 100042-07 | Width 20.3 cm | Withdrawn |
| 100042-01 | Length 15.5 cm | Withdrawn |
| 100042-11 | Height 10.2 cm | Withdrawn |
| 100042-10 | Length 2.5 cm | Withdrawn |
| 100042-08 | Length 7.6 cm | Withdrawn |
| 100042-06 | Height 7.5 cm | Withdrawn |
| 100042-03 | Length 18.5 cm | Withdrawn |
| 100042-05 | Length 21.0 cm | Withdrawn |
| 100042-14 | Outer Diameter 7.6 cm | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Phasix | Davol Inc. | 37 |
| GalaFLEX Scaffold | Tepha, Incorporated | 14 |
| GalaFLEX Lite | Tepha, Incorporated | 14 |
| GalaFLEX 3D | Tepha, Incorporated | 14 |
| GalaFLEX Lite | Davol Inc. | 13 |
| GalaFLEX 3DR | Tepha, Incorporated | 13 |
| GalaFORM 3D | Tepha, Incorporated | 13 |
| GalaFLEX 3D | Davol Inc. | 7 |
| GalaFLEX 3DR | Davol Inc. | 6 |
| GalaFLEX | Davol Inc. | 5 |
| Gelfilm | Pharmacia & Upjohn Company LLC | 2 |
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K233999 | 2024-04-09 |
| K202425 | 2021-08-19 |
| K162922 | 2017-02-23 |
| K161092 | 2016-08-23 |
| K140533 | 2014-05-21 |
| K130326 | 2013-05-07 |
| K113723 | 2012-02-15 |
| K113721 | 2012-02-15 |
| K111946 | 2011-09-26 |
| K091633 | 2009-08-07 |
| K070894 | 2007-04-13 |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2016-11-21 | Class II | Process design | Endotoxin values from testing of retains slightly exceeded the established specification. | 29 | 2017-01-05 |
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.