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Excella® Navigation

FDA UDI

Class II (US FDA UDI)

by Innovasis, Inc.

Identity

Trade Name
Excella® Navigation FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
Bone Tap, 5.0mm, Cannulated, MedT Nav, SST FDA UDI
Model / Reference
LS-695 FDA UDI
Description
Bone Tap, 5.0mm, Cannulated, MedT Nav, SST FDA UDI

Identifiers

Primary DI / UDI-DI
M711LS6950 FDA UDI
510(k) Number
K223511 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Bone tap, reusable 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 5 Millimeter FDA UDI

Category: Bone tap, reusable

Excella® Navigation by Innovasis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innovasis, Inc.

Sources (1)

  • FDA UDI a088e514-1ff3-4126-9b84-8669750b57a4 36 fields · synced May 30, 2026