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Tecomet SP101316

by Tecomet, Inc

Tecomet SP101316 is a Class I device made by Tecomet, Inc, listed in FDA GUDID since 7 Oct 2020 (UDI-DI 00818069016760), 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 Number00818069016760 UDI-DI Date7 Oct 2020ListedStatusListed 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  • Withdrawn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
Tecomet
Generic name
Endoscopic surgical probe
Model / reference
SP101316
Primary DI / UDI-DI
00818069016760
FDA product code
HXB
GMDN term
Endoscopic surgical probe
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscopic surgical probe

Similar devices in this category

Other devices filed under Endoscopic surgical probe.

Other devices from Tecomet, Inc

See all devices from Tecomet, Inc →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)