← Back to catalogue

Silhouette Lift

FDA UDI

Class II (US FDA UDI)

by Sinclair Pharma US Inc.

Identity

Trade Name
Silhouette Lift FDA UDI
Generic Name
Lift thread, partially-bioabsorbable FDA UDI
Device Name
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 40.5 cm in length, with a total of 6 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. FDA UDI
Model / Reference
SMS 01-PP-3.0.1-B-S FDA UDI
Description
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 40.5 cm in length, with a total of 6 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. FDA UDI

Identifiers

Primary DI / UDI-DI
05060033040171 FDA UDI
510(k) Number
K060414 FDA UDI
K171005 FDA UDI
FDA Product Code
GAW FDA UDI
GAM FDA UDI
GMDN Term
Lift thread, partially-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5010 FDA UDI
878.4493 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Lift thread, partially-bioabsorbable

Silhouette Lift by Sinclair Pharma US Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sinclair Pharma US Inc.

Sources (1)

  • FDA UDI 2bf1be51-2086-475b-aa48-99eefbd187f4 36 fields · synced May 30, 2026