Uniester C
FDA 510(k) K042286 · United Medical Industries Co. , Ltd.
510(k) numberK042286
Submission
- Device name
- Uniester C
- Applicant
- United Medical Industries Co. , Ltd.
Riyadh, Central Province, SA - Received
- August 24, 2004
- Decision date
- December 1, 2004
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- GAT – Suture, Nonabsorbable, Synthetic, Polyethylene
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.5000
- Specialty
- General, Plastic Surgery
- Implant
- Yes
Other 510(k)s with product code GAT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253910 | Stitch - Suture Wires and TapesGAT · Traditional | GM Dos Reis Industria e Comercio Ltda. | 08/22/2026SE |
| K261021 | EasyWhip FamilyGAT · Traditional | Winter Innovations, Inc. | 07/01/2026SE |
| K260775 | Polyethylene;Polyethylene Fusion;Polyethylene OrthoTapeGAT · Traditional | Teleflex Medical, LLC | 05/06/2026SE |
| K254275 | HyperSuture All Green Extension LineGAT · Traditional | Threadstone, LLC | 03/23/2026SE |
| K254188 | Meniscus VersaflexGAT · Traditional | GM Dos Reis Industria e Comercio Ltda. | 02/19/2026SE |
| K253145 | Pre-Sutured TendonGAT · Special | Rti Surgical, Inc. | 10/22/2025SE |
| K253024 | ProZip Knotless ImplantGAT · Special | Riverpoint Medical | 10/16/2025SE |
| K252225 | PowerKnot High Strength SuturesGAT · Traditional | Medacta International S.A. | 09/12/2025SE |
| K252201 | HS FiberGAT · Special | Riverpoint Medical | 08/13/2025SE |
| K242201 | HyperSuture White/Green Extension LineGAT · Traditional | Threadstone, LLC | 03/27/2025SE |
More from Threadstone, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K072646 | UnicaproneGAM · Traditional | 11/07/2007SE |
| K072645 | UniglactinGAM · Traditional | 11/07/2007SE |
| K072644 | Unicryl QuickGAM · Traditional | 11/07/2007SE |
| K042287 | Uniplain & UnichromGAL · Traditional | 09/07/2005SE |
| K042288 | UnicrylGAM · Traditional | 12/27/2004SE |
| K042285 | Unicryl MNEW · Traditional | 12/10/2004SE |
| K042284 | UnimideGAR · Traditional | 12/03/2004SE |
| K042283 | UniproGAW · Traditional | 12/01/2004SE |
| K042282 | UnisilkGAP · Traditional | 12/01/2004SE |
Questions and answers
When was Uniester C cleared by the FDA?
Uniester C (K042286) received a 510(k) decision of Substantially Equivalent on December 1, 2004, 99 days after the submission was received.
What is the product code of K042286?
The FDA product code is GAT – Suture, Nonabsorbable, Synthetic, Polyethylene, a Class II (moderate risk) device regulated under 21 CFR 878.5000.