← Back to catalogue

Recon

FDA UDI

Class I (US FDA UDI)

by Revelation Medical Devices, Llc

Identity

Trade Name
Recon FDA UDI
Generic Name
General-purpose curette FDA UDI
Device Name
Long 12" Curette Sz 4 FDA UDI
Model / Reference
10-883-20-4 FDA UDI
Description
Long 12" Curette Sz 4 FDA UDI

Identifiers

Catalog Number
10-883-20-4 FDA UDI
Primary DI / UDI-DI
G318108832040 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
General-purpose curette FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

No

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: General-purpose curette

Recon is a hand-held, manual surgical instrument designed for scraping and/or excising tissue from various anatomical sites. With its high-grade stainless steel construction and appropriately-shaped distal end, this single-use device is ideal for general-purpose use in medical procedures.

Similar devices

Also classified as General-purpose curette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f76779e5-7fab-4749-8728-a8f458b63389 35 fields · synced Jul 24, 2026