3DMAX

3DMax MID Anatomical Mesh, 12 cm x 17 cm (5" x 7"), Extra Large, Right

Registry build 21.09.26
1manufacturer
18catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code FTL
Manufacturer City Province Registered as Device types
Shanghai Suokang Medical Implants Co., Ltd. Shang Hai Shanghai Manufacturer 2

Record

Regulatory record for 3DMAX
Listed by Davol Inc., United States
FDA product code FTL
Device type Mesh, Surgical, Polymeric
Device class Class 2
Regulation 21 CFR 878.3300
Establishment Manufacturer
Record published 2020-07-27
Record revised 2025-08-18 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Sizes Width 7.9 to 12.4 cm; length 13 to 17.3 cm

Catalogue Numbers

Catalogue numbers for 3DMAX
Catalogue number Size Status
0116310 Width 8 cm In distribution
0117322 Length 17.0 cm In distribution
0117310 Width 7.9 cm In distribution
0115321 Length 16.0 cm In distribution
0116321 Length 16 cm In distribution
0116320 Length 13 cm In distribution
0117321 Width 10.3 cm In distribution
0115320 Width 8.5 cm In distribution
0115310 Length 13.7 cm In distribution
0115312 Length 17.3 cm In distribution
0115322 Width 12.4 cm In distribution
0117311 Length 15.7 cm In distribution
0116312 Length 17 cm In distribution
0116322 Length 17 cm In distribution
0117320 Length 13.4 cm In distribution
0116311 Length 16 cm In distribution
0115311 Width 10.8 cm In distribution
0117312 Length 17.0 cm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Technical Products Technical Products, Inc. 143
Parietex Sofradim Production 82
DynaMesh FEG Textiltechnik Forschungs- und Entwicklungsges. mbH 45
Symbotex Sofradim Production 35
Silicone Sheeting Reinforced Bentec Medical OpCo, LLC. 33
Parietene Sofradim Production 32
C-QUR Atrium Medical Corporation 31
ProGrip Sofradim Production 31
Silicone Sheeting Non-Reinforced Bentec Medical OpCo, LLC. 31
Prolite Atrium Medical Corporation 31
Gore Seamguard Bioabsorbable Staple Line Reinforce W. L. Gore & Associates, Inc. 30
Surgimesh®wn Aspide Medical 28

Showing 12 of 148. All products under Mesh, Surgical, Polymeric

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K251557 2025-06-12
K250098 2025-04-09
K003323 2001-01-22
K792281 1979-11-27

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P990028 2003-12-04 FOCALSEAL-L SYNTHETIC ABSORBABLE SEALANT Genzyme Corporation

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