Identity
- Trade Name
- Lantern FDA UDI
- Generic Name
- Orthopaedic stereotactic surgery system FDA UDI
- Device Name
- Packaged Assembly, Nav Unit, LSA Hip FDA UDI
- Model / Reference
- 502000-01 FDA UDI
- Description
- Packaged Assembly, Nav Unit, LSA Hip FDA UDI
Identifiers
- Catalog Number
- 502000-01 FDA UDI
- Primary DI / UDI-DI
- 00810832031994 FDA UDI
- 510(k) Number
- K242616 FDA UDI
- FDA Product Code
- ONN FDA UDI
- GMDN Term
- Orthopaedic stereotactic surgery system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Orthopaedic stereotactic surgery system
Lantern by Orthalign, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic stereotactic surgery system.
- TRIGEN — Smith & Nephew, Inc. · Class II
- PULSE — Nuvasive, Inc. · Class II
- KneePlus — PIXEE MEDICAL · Class II
- intellijoint HIP® — Intellijoint Surgical Inc · Class II
- PULSE — Nuvasive, Inc. · Class II
- Navigation Unit Kit — GYDER SURGICAL PTY LTD · Class II
- StealthStation S8 Spine — MEDTRONIC NAVIGATION, INC. · Class II
- WatchTower — Intai Technology Corporation · Class II
Cleared under the same submission
K242616 also covers:
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, Inc.
- Lantern — Orthalign, 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
- Orthalign, Inc.
Sources (1)
- FDA UDI 432e38c5-7f3c-4b9d-9c71-86eba3c12735 37 fields · synced May 30, 2026