Identity
- Trade Name
- ADVANTIME FDA UDI
- Generic Name
- Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI
- Model / Reference
- 15D10G FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03661522031278 FDA UDI
- 510(k) Number
- K232372 FDA UDI
- FDA Product Code
- GAM FDA UDI
- GMDN Term
- Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4493 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
Yes
Contains Latex
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
Yes
Category: Polyester suture, bioabsorbable, monofilament, non-antimicrobial
ADVANTIME is a high-quality, single-use polyester suture designed for general surgical applications. Its unique monofilament construction and bioabsorbable properties make it an ideal choice for wound closure, minimizing the need for subsequent stitches or sutures.
Similar devices
Also classified as Polyester suture, bioabsorbable, monofilament, non-antimicrobial.
- Monoswift — RIVERPOINT MEDICAL LLC · Class II
- DemeDIOX — DemeTECH Corp · Class II
- DemeCAPRONE — DemeTECH Corp · Class II
- DemeCAPRONE — DemeTECH Corp · Class II
- WEGO-PDO Absorbable Surgical Suture With Needle — Foosin Medical Supplies, Inc. · Class II
- Maxon — Covidien LP · Class II
- DemeCAPRONE — DemeTECH Corp · Class II
- DemeCAPRONE — DemeTECH Corp · Class II
Cleared under the same submission
K232372 also covers:
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
- ADVANTIME — PETERS SURGICAL
Authorization Coverage (1 country)
Regulatory Authorizations
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Peters Surgical
Sources (1)
- FDA UDI b9cdc8c9-46bf-4a77-859c-51d163464df8 33 fields · synced Jun 20, 2026