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SunMed 8-1053-85

by SunMed

SunMed 8-1053-85 is a medical device (FDA Class II; FDA product code BXN, Stimulator, Nerve, Battery-Powered) made by SunMed, cleared under FDA 510(k) K153045 on 13 May 2016 and listed in FDA GUDID since 1 Aug 2023 (UDI-DI 10889483000014), active as of 23 Oct 2026.

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

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K153045

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10889483000014 UDI-DI Date1 Aug 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK153045 Date13 May 2016DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K153045 decided 13 May 2016 Active
  • FDA GUDID UDI-DI 10889483000014 listed 1 Aug 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K153045
  2. Listed FDA GUDID 10889483000014

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
SunMed
Generic name
Block-monitoring peripheral nerve electrical stimulation system
Model / Ref / Catalog
8-1053-85
Primary DI / UDI-DI
10889483000014
510(k) Number
FDA product code
BXN
GMDN term
Block-monitoring peripheral nerve electrical stimulation system
Device class
Class II
Regulation number
868.2775
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code BXN (STIMULATOR, NERVE, BATTERY-POWERED).

Other devices from SunMed

See all devices from SunMed →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)