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Large Bone Caliper 01293

by Lafayette Instrument Company

Large Bone Caliper 01293 is a general-purpose calliper (FDA Class I; FDA product code KTZ, Caliper) made by Lafayette Instrument Company, listed in FDA GUDID since 31 Aug 2021 (UDI-DI 00855170007034), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00855170007034 UDI-DI Date31 Aug 2021ListedStatusListed 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  • Withdrawn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
Large Bone Caliper
Generic name
General-purpose calliper, plastic
Model / Ref / Catalog
01293
Primary DI / UDI-DI
00855170007034
FDA product code
KTZ
GMDN term
General-purpose calliper, plastic
Device class
Class I
Regulation number
888.4150
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KTZ (Caliper).

Other devices from Lafayette Instrument Company

See all devices from Lafayette Instrument Company →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)