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Canaveral®

FDA UDI

Class II (US FDA UDI)

by Flospine

Identity

Trade Name
Canaveral® FDA UDI
Generic Name
Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI
Device Name
Rod Holder vice grips FDA UDI
Model / Reference
Canaveral® FDA UDI
Description
Rod Holder vice grips FDA UDI

Identifiers

Catalog Number
01-7000-032 FDA UDI
Primary DI / UDI-DI
B183170000320 FDA UDI
510(k) Number
K141850 FDA UDI
FDA Product Code
KWP FDA UDI
NKB FDA UDI
OSH FDA UDI
MNH FDA UDI
MNI FDA UDI
GMDN Term
Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
888.3070 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Abdominal/ENT/orthopaedic surgical probe, reusable

Canaveral® by Flospine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal/ENT/orthopaedic surgical probe, reusable.

Cleared under the same submission

K141850 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flospine

Sources (1)

  • FDA UDI bc9ea6c5-ec85-4403-9bde-970928c2b06e 36 fields · synced Jun 1, 2026