Identity
- Trade Name
- Simpact Tri-Fin FDA UDI
- Generic Name
- Bone curette, reusable FDA UDI
- Device Name
- Anterior Curette #1 Ang 9" Handle FDA UDI
- Model / Reference
- 710-1801-1 FDA UDI
- Description
- Anterior Curette #1 Ang 9" Handle FDA UDI
Identifiers
- Catalog Number
- 710-1801-1 FDA UDI
- Primary DI / UDI-DI
- 00190837063337 FDA UDI
- 510(k) Number
- K141246 FDA UDI
- FDA Product Code
- OUR FDA UDI
- GMDN Term
- Bone curette, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone curette, reusable
Simpact Tri-Fin by Life Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone curette, reusable.
- Symmetry Bruns — SYMMETRY SURGICAL INC. · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- Spinal System — BIOMET SPINE LLC · Class I
- Life Instruments — Life Instrument Corporation · Class I
- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- Volkmann Bone Curette Oval - Fig. 00 17 cm - 6 3/4" Scoop Size 4.4 mm Stainless Steel — SURTEX INSTRUMENTS LTD · Class I
Cleared under the same submission
K141246 also covers:
- Simpact — Life Spine, Inc.
- Simpact — Life Spine, Inc.
- Simpact — Life Spine, Inc.
- Simpact — Life Spine, Inc.
- Simpact — Life Spine, Inc.
- Simpact — Life Spine, Inc.
- Simpact — Life Spine, Inc.
- Simpact — Life Spine, Inc.
- Simpact Sacroiliac Joint Compression Screw System — Life Spine, Inc.
- Simpact Sacroiliac Joint Compression Screw System — Life Spine, Inc.
- Simpact Sacroiliac Joint Compression Screw System — Life Spine, Inc.
- Simpact Sacroiliac Joint Compression Screw System — Life Spine, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
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
- Life Spine, Inc.
Sources (1)
- FDA UDI dd377ec0-f71d-4aa2-a182-3bc27d63cc03 35 fields · synced May 29, 2026