PerFix
PerFix Light Plug, 1.5" x 2.0" (3.8 cm x 5.0 cm), Extra Large (Contents: 6)
1manufacturer
16catalogue numbers in this listing
4510(k) clearances naming this product code
Who Else Makes It
Registered in Shanghai.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shanghai Suokang Medical Implants Co., Ltd. | Shang Hai | Shanghai | Manufacturer | 2 |
Record
| 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 | 2015-08-06 |
| Record revised | 2025-08-18 (version 8) |
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 |
| Packaging | Case of 6, case of 2 |
| Sizes | Height 2.5 to 4.1 cm; outer diameter 3.4 to 5 cm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 0117170 | Height 4.1 cm | In distribution |
| 0112980 | Height 3.8 cm | In distribution |
| 0112960 | Height 3.3 cm | In distribution |
| 0112750 | Height 2.5 cm | In distribution |
| 0112950 | Height 2.5 cm | In distribution |
| 0112780 | Outer Diameter 5.0 cm | In distribution |
| 0112770 | Outer Diameter 4.8 cm | In distribution |
| 0112760 | Height 3.3 cm | In distribution |
| 0112970 | Height 4.1 cm | In distribution |
| 0117160 | Height 3.3 cm | In distribution |
| 0117060 | Outer Diameter 3.9 cm | In distribution |
| 0117150 | Height 2.5 cm | In distribution |
| 0117180 | Height 3.8 cm | In distribution |
| 0117080 | Height 3.8 cm | In distribution |
| 0117050 | Outer Diameter 3.4 cm | In distribution |
| 0117070 | Outer Diameter 4.8 cm | In distribution |
Same 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
| 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.
| 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.