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6501

by Boston Scientific 2 variants

6501 (666501-105) is a Class III device made by Boston Scientific, approved under FDA PMA P930035 on 10 Mar 1995 and listed in FDA GUDID since 8 Nov 2018 (UDI-DI 00802526605901), active as of 22 Oct 2026.

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

PMA

Valid until

No expiry

PMA approval is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

PMA P930035

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00802526605901 UDI-DI Date8 Nov 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA PMAAPPR from GUDID Approved NumberP930035 Date10 Mar 1995DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA PMA P930035 decided 10 Mar 1995 Active
  • FDA GUDID UDI-DI 00802526605901 listed 8 Nov 2018 Listed

Timeline

2 dated events

  1. Approved FDA PMA P930035
  2. Listed FDA GUDID 00802526605901

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA PMA Active

Specification

GUDID

Generic name
Surgical torque wrench, single-use
Model / Ref / Catalog
6501, 666501-105
Primary DI / UDI-DI
00802526605901
PMA number
FDA product code
LWS
GMDN term
Surgical torque wrench, single-use
Device class
Class III
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical torque wrench, single-use

Cleared under the same submission (P930035)

Other devices from Boston Scientific

See all devices from Boston Scientific →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)