Identity
- Trade Name
- Peri-Loc FDA UDI
- Generic Name
- Surgical depth gauge, reusable FDA UDI
- Device Name
- 3.5MM SCREW DEPTH GAUGE FDA UDI
- Model / Reference
- 71173534 FDA UDI
- Description
- 3.5MM SCREW DEPTH GAUGE FDA UDI
Identifiers
- Catalog Number
- 71173534 FDA UDI
- Primary DI / UDI-DI
- 03596010519993 FDA UDI
- 510(k) Number
- K093047 FDA UDI
- FDA Product Code
- KTT FDA UDI
- GMDN Term
- Surgical depth gauge, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 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: Surgical depth gauge, reusable
Peri-Loc by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical depth gauge, reusable.
- Depth Gauge — I.T.S. GmbH · Class I
- FO NX Nail System — FIELD ORTHOPAEDICS PTY LTD · Class I
- FO Micro Screw System — FIELD ORTHOPAEDICS PTY LTD · Class I
- Summa Orthopaedics System Surgical Instrument — Jeil Medical Corporation · Class I
- HOOK TIP DEPTH GAUGE CLAVICLE SYSTEM — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class I
- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- Summa Orthopaedics System Surgical Instrument — Jeil Medical Corporation · Class I
- Arthrex® — Arthrex, Inc. · Class I
Cleared under the same submission
K093047 also covers:
- Anthology — Smith & Nephew, Inc.
- CHS — Smith & Nephew, Inc.
- CHS — Smith & Nephew, Inc.
- Ex-Fix — Smith & Nephew, Inc.
- Ex-Fix — Smith & Nephew, Inc.
- ILIZAROV — Smith & Nephew, Inc.
- ILIZAROV SYSTEMS — Smith & Nephew, Inc.
- IMHS — Smith & Nephew, Inc.
- IMHS — Smith & Nephew, Inc.
- Jet-X — Smith & Nephew, Inc.
- Jet-X — Smith & Nephew, Inc.
- Jet-X — 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 |
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Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI f4b9dc18-391a-4f9a-a047-053b3fed4aca 36 fields · synced Jun 8, 2026