Revcon VDB01000

by Voom Medical Devices, Inc

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

in data synced 9 Nov 2026

Documents

FDA submission, from GUDID

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 9 Nov 2026. What this means

Regulatory status

as of registry sync 9 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00850041704081 UDI-DI	Date5 Apr 2023Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK223392	Date28 Feb 2023Decided	StatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 9 Nov 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Revcon
Generic name: Cannulated surgical drill bit, reusable
Model / Ref / Catalog: VDB01000

Primary DI / UDI-DI: 00850041704081
510(k) Number: K223392
FDA product code: HWC
GMDN term: Cannulated surgical drill bit, reusable

Device class: Class II
Regulation number: 888.3040
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Size: Outer Diameter — 2.2 Millimeter

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Revcon RSN3042

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Voom Medical REVCONTM Screw System RSA4048

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Voom Medical REVCONTM Screw System RSA4050

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See all devices from Voom Medical Devices, Inc →

Properties

Sterilise before use
Prescription use
Lot / batch number

Other properties (12)

Supplied sterile: No
Single use: No
Implantable: No
Contains latex: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Premarket exempt: No
Serial number: No
Expiration date: No
Manufacturing date: No