What is FDA product code OOD?

To be implanted to reinforce soft tissue or bone where weakness exists. Intended to be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological, or gastrointestinal anatomy, or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. The absorbable protective film also may help minimize the potential for tissue attachment to the device in case of direct contact with the viscera.

General & Plastic Surgery › ProstheticSurgical Film

GalaFLEX Scaffold

Name: GalaFLEX Scaffold
Brand: GalaFLEX Scaffold

GalaFLEX Scaffold is a resorbable surgical mesh used as a temporary scaffold for soft tissue support. It is placed to repair, elevate or reinforce tissue where weakness or a void requires…

Registry build 21.09.26

GalaFLEX Scaffold is a resorbable surgical mesh used as a temporary scaffold for soft tissue support. It is placed to repair, elevate or reinforce tissue where weakness or a void requires additional supporting material.

Its applications include reinforcement of soft tissue in plastic and reconstructive surgery and general soft tissue reconstruction. The mesh is supplied as individual sheets in different widths, lengths and shapes, and can be cut to suit the surgical application.

Listed Item

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

Mesh Construction

The sterile mesh is knitted from undyed monofilament fibers of poly-4-hydroxybutyrate, also called P4HB. This polymer forms the resorbable structure of the scaffold.

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 GalaFLEX Scaffold
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
510(k)	K140533
Record published	2016-05-27
Record revised	2025-11-24 (version 10)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Sterilisation	Ethylene Oxide
Supplied sterile	Yes
Single use	Yes
Prescription	Prescription only
Latex	Contains natural rubber latex
Label carries	lot or batch number, expiry date
Storage	Storage environment temperature 15 to 25 °C
Sizes	Width 2.5 to 15 cm; length 2.5 to 26 cm
Distribution end date	2021-07-26

Catalogue Numbers

Catalogue numbers for GalaFLEX Scaffold
Catalogue number	Size	Status
100035-01	Width 5 cm	In distribution
100035-15	Length 20 cm	In distribution
100035-09	Length 20 cm	In distribution
100035-05	Length 7.6 cm	In distribution
100035-14	Length 20 cm	In distribution
100035-20	Width 9 cm	Withdrawn
100035-26	Width 8.5 cm	Withdrawn
100035-29	Width 7.7 cm	Withdrawn
100035-23	Width 10 cm	Withdrawn
100035-17	Width 10 cm	Withdrawn
100035-25	Width 10 cm	Withdrawn
100035-22	Width 11.8 cm	Withdrawn
100035-28	Width 10 cm	Withdrawn
100035-19	Width 10.6 cm	Withdrawn

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Phasix	Davol Inc.	37
GalaFLEX Lite	Tepha, Incorporated	14
GalaFLEX 3D	Tepha, Incorporated	14
GalaSHAPE 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.