GalaSHAPE 3d

GalaSHAPE 3D scaffold is a bioresorbable surgical mesh manufactured from poly-4-hydroxybutyrate (P4HB).

Registry build 21.09.26
1manufacturer
14catalogue numbers in this listing
11510(k) clearances naming this product code
1recall

Who Else Makes It

Registered in Fujian.

Chinese manufacturers registered for FDA product code OOD
Manufacturer City Province Registered as Device types
Xiamen MK Health Care Product Co., Ltd. Xiamen Fujian Manufacturer 7

Record

Regulatory record for GalaSHAPE 3D
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

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 numbers for GalaSHAPE 3D
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100042-12 Height 10.2 cm Withdrawn
100042-02 Height 5.3 cm Withdrawn
100042-04 Height 6.4 cm Withdrawn
100042-09 Width 7.6 cm Withdrawn
100042-13 Outer Diameter 7.6 cm Withdrawn
100042-07 Width 20.3 cm Withdrawn
100042-01 Length 15.5 cm Withdrawn
100042-11 Height 10.2 cm Withdrawn
100042-10 Length 2.5 cm Withdrawn
100042-08 Length 7.6 cm Withdrawn
100042-06 Height 7.5 cm Withdrawn
100042-03 Length 18.5 cm Withdrawn
100042-05 Length 21.0 cm Withdrawn
100042-14 Outer Diameter 7.6 cm Withdrawn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

Other products under the same FDA 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

FDA 510(k) clearances naming this product code
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.

Recalls referencing this product code
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.

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