510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K001808Substantially Equivalent

Doro Headrest System

Black Forest Medical GmbH, Roswell GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001808 is the FDA 510(k) clearance record for DORO HEADREST SYSTEM, a class II device, cleared for Pro-Med Instruments GmbH on under FDA product code HBL (Holder, Head, Neurosurgical (Skull Clamp)). FDA records list 10 510(k) clearances for Black Forest Medical GmbH, from to . As of , FDA records show 2 recalls naming K001808.

Clearance record

Decision date
Received
(50 days to decision)
Product code
HBL Holder, Head, Neurosurgical (Skull Clamp)
Regulation
21 CFR 882.4460
Device class
Class II
Review panel
Neurology
Applicant
Pro-Med Instruments GmbH 9070 Bluffview Trace, Roswell GA
510(k) summary
Summary
Third party review
No

Clearances, product code HBL

Trailing 12 months
1 clearance under product code HBL in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HBL, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260