Skip to content

Integra® INS7040

by Integra Pain Management 2 variants

Integra® INS7040 is a device made by Integra Pain Management, listed in FDA GUDID since 3 Nov 2017 (UDI-DI 10381780431909), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10381780431909 UDI-DI Date3 Nov 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Integra®
Generic name
Manual cranial rotary handpiece, single-use
Model / Ref / Catalog
INS7040
Primary DI / UDI-DI
10381780431909
GMDN term
Manual cranial rotary handpiece, single-use
GUDID distribution status
In Commercial Distribution

Related devices

Category: Manual cranial rotary handpiece, single-use

Other devices from Integra Pain Management

See all devices from Integra Pain Management →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Combination product
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)