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Renovo Life, LLC

FDA UDI

Class I (US FDA UDI)

by Renovo Life, LLC

Identity

Trade Name
Renovo Life, LLC FDA UDI
Generic Name
Fluted surgical drill bit, single-use, non-sterile FDA UDI
Device Name
3.5mm Drill Bit, Quick Connect, 110mm length FDA UDI
Model / Reference
RNL-310-350 FDA UDI
Description
3.5mm Drill Bit, Quick Connect, 110mm length FDA UDI

Identifiers

Catalog Number
RNL-310-350 FDA UDI
Primary DI / UDI-DI
M734RNL3103500 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Fluted surgical drill bit, single-use, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fluted surgical drill bit, single-use, non-sterile

Renovo Life, LLC by Renovo Life, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Renovo Life, LLC

Sources (1)

  • FDA UDI 3129d05e-d3f8-463e-b7ce-f3ac7e94ac7b 35 fields · synced May 29, 2026