Silhouette Lift

Silhouette Lift suture is a non-absorbable polypropylene suture with an implantable grade L-lactide/Glycolide (PLG-8218) resorbable based cone that has been injection molded to strict…

Registry build 21.09.26

Silhouette Lift suture is a non-absorbable polypropylene suture with an implantable grade L-lactide/Glycolide (PLG-8218) resorbable based cone that has been injection molded to strict tolerances and affixed to the polypropylene base suture in a secondary operation without any modification or degradation to the base suture. This model number of Silhouette Lift suture is 37.3 cm in length, with a total of 10 molded cones fixed to the distal end of the suture. Silhouette Lift suture is indicated for use in mid-face suspension surgery to fixate the cheek dermis in an elevated position.

3manufacturers in China registered for this device type
3catalogue numbers in this listing

Who Else Makes It

Concentrated in Shandong (2), Beijing (1).

Chinese manufacturers registered for FDA product code GAW
Manufacturer City Province Registered as Device types
Shandong Haidike Medical Products Co., Ltd. Heze Shandong Manufacturer 22
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8
ARC Medical Supplies (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7

Record

Regulatory record for Silhouette Lift
Listed by Sinclair Pharma US, Inc., United States
FDA product code GAW
Device type Suture, Nonabsorbable, Synthetic, Polypropylene
Device class Class 2
Regulation 21 CFR 878.5010
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K060414
Record published 2015-09-24
Record revised 2022-05-23 (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
Storage Storage environment temperature 0 to 27 °C
Packaging Dispenser box of 10, dispener box of 10
Distribution end date 2020-07-31
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Silhouette Lift
Catalogue number Size Per pack Status
SMS 01-PP-3.0.1-B-S 2 In distribution
SMS 02-PP-2.0.1-B 2 Withdrawn
SMS 03-PP-3.0.1-CL 2 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DemeLENE Demetech Corp. 1,707
Premilene B Braun Surgical SA 1,247
Optilene B Braun Surgical SA 1,110
Prolene Ethicon, Inc. 765
Deknatel Teleflex Medical LLC 373
Corolene® Peters Surgical 354
WEGO-Polypropylene Nonabsorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 346
Surgipro II Covidien LP 254
Surgipro ll Covidien LP 152
Atramat Internacional Farmacéutica S.A DE C.V 140
Surgipro Covidien LP 133
Filaprop Meril Endo Surgery PVT. Ltd. 123

Showing 12 of 200. All products under Suture, Nonabsorbable, Synthetic, Polypropylene

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Silhouette Lift
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Sinclair Pharma US, Inc. 510(k) number 2015-07-02 Class II Labeling False and Misleading Silhouette Lift is recalling the Silhouette Suture brochure because it does not include a complete list of risks and side effects. Therefore, it can potentially mislead the patient regarding the safety of the product. 2,260 units 2016-02-05

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
P890002 1989-05-31 POLYPROPYLENE SURGICAL SUTURE Alcon Laboratories, Inc.
P820083 1986-08-05 GORE-TEX(R) EXPANDED PTFE SUTURE W. L. Gore & Associates, Inc.

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