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Shard A750-BP60

by Applied Dental, Inc.

Shard A750-BP60 is a Class I device made by Applied Dental, Inc., listed in FDA GUDID since 16 Mar 2022 (UDI-DI 00814639025194), 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 Number00814639025194 UDI-DI Date16 Mar 2022ListedStatusListed 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  • Withdrawn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
Shard
Generic name
Skin-coring punch, single-use
Model / Ref / Catalog
A750-BP60
Description
Disposable Stainless Steel Biopsy Punch Sterile. 6.0mm.
Primary DI / UDI-DI
00814639025194
FDA product code
EME
GMDN term
Skin-coring punch, single-use
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin-coring punch, single-use

Similar devices

Other devices filed under FDA product code EME (Punch, Biopsy, Surgical).

Other devices from Applied Dental, Inc.

See all devices from Applied Dental, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)