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Bovie

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Bovie FDA UDI
Generic Name
Electrocautery system generator, battery-powered FDA UDI
Device Name
Cautery Adjust-A-Temp Low Temp Fine Tip (10/bx) FDA UDI
Model / Reference
AA02 FDA UDI
Description
Cautery Adjust-A-Temp Low Temp Fine Tip (10/bx) FDA UDI

Identifiers

Primary DI / UDI-DI
10887482177171 FDA UDI
510(k) Number
K945762 FDA UDI
FDA Product Code
HQP FDA UDI
GMDN Term
Electrocautery system generator, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4115 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocautery system generator, battery-powered

Bovie by Symmetry Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocautery system generator, battery-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI 292f65f3-a1dc-4429-8369-0dae14e9b5d9 36 fields · synced Jun 8, 2026