Identity
- Trade Name
- Excella MIS® FDA UDI
- Generic Name
- Bone access cannula FDA UDI
- Device Name
- SST FDA UDI
- Model / Reference
- LS-278 FDA UDI
- Description
- SST FDA UDI
Identifiers
- Catalog Number
- LS-278 FDA UDI
- Primary DI / UDI-DI
- M711LS2780 FDA UDI
- 510(k) Number
- K102248 FDA UDI
- FDA Product Code
- NKB FDA UDIMNI FDA UDIMNH FDA UDIKWP FDA UDIKWQ FDA UDI
- GMDN Term
- Bone access cannula FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 FDA UDI888.3050 FDA UDI888.3060 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 6 Inch FDA UDINeedle Gauge — 11 Gauge FDA UDI
Category: Bone access cannula
Excella MIS® by Innovasis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone access cannula.
- BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length — Tecres · Class I
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- Arthrex® — Arthrex, Inc. · Class I
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- Boston Endo Surgical Technologies LLC — LACEY MANUFACTURING COMPANY LLC · Class II
- Boston Endo Surgical Technologies LLC — LACEY MANUFACTURING COMPANY LLC · Class II
Cleared under the same submission
K102248 also covers:
- Excella 3® — Innovasis, Inc.
- Excella 3® — Innovasis, Inc.
- Excella 3® — Innovasis, Inc.
- Excella 3® — Innovasis, Inc.
- Excella 3® — Innovasis, Inc.
- Excella 3® — Innovasis, Inc.
- Excella 3® — Innovasis, Inc.
- Excella 3® — Innovasis, Inc.
- Excella 3® — Innovasis, Inc.
- Excella 3® — Innovasis, Inc.
- Excella 3™ — Innovasis, Inc.
- Excella 3™ — Innovasis, 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
- Innovasis, Inc.
Sources (1)
- FDA UDI 4f8eeeeb-fa50-4172-9dbd-661aa87c14e9 37 fields · synced May 30, 2026