Identity
- Trade Name
- TC-100 FDA UDI
- Generic Name
- Bone holding forceps FDA UDI
- Device Name
- SELF-CENTERING FORCEPS W/ SPEED LOCK 240MM FDA UDI
- Model / Reference
- 71170046 FDA UDI
- Description
- SELF-CENTERING FORCEPS W/ SPEED LOCK 240MM FDA UDI
Identifiers
- Catalog Number
- 71170046 FDA UDI
- Primary DI / UDI-DI
- 03596010180797 FDA UDI
- 510(k) Number
- K123598 FDA UDI
- FDA Product Code
- JDG FDA UDI
- GMDN Term
- Bone holding forceps FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3360 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 holding forceps
Tc-100 by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone holding forceps.
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- gSource — GSOURCE, LLC. · Class I
- Thrust Arm, Left, Pelvic Linear Hook Attachment — I.T.S. GmbH · Class I
- FORCEPS — KLS-Martin L.P. · Class I
- Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
- CLAMP — KLS-Martin L.P. · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Tecomet — Tecomet,Inc · Class I
Cleared under the same submission
K123598 also covers:
- 'SL-PLUS¿' — Smith & Nephew, Inc.
- ANTHOLOGY — Smith & Nephew, Inc.
- ANTHOLOGY — Smith & Nephew, Inc.
- Accord — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- CATALYSTEM — Smith & Nephew, Inc.
- CONTOUR — Smith & Nephew, 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
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 787a401d-3994-4cf9-917e-ffb6649b5373 36 fields · synced Jun 8, 2026